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Loraine Klein Phones & Addresses

  • 331 Somerset Dr, Streamwood, IL 60107 (630) 837-3425
  • Bensenville, IL
  • Carol Stream, IL

Resumes

Resumes

Loraine Klein Photo 1

Loraine Klein

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Location:
Greater Chicago Area
Industry:
Chemicals
Loraine Klein Photo 2

Project Management Institute

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Location:
331 Somerset Dr, Streamwood, IL 60107
Industry:
Chemicals
Work:

Project Management Institute
Education:
Project Management Institute 2015 - 2025
Michigan State University 1976 - 1980
Bachelors, Bachelor of Science, Chemical Engineering
Skills:
Presentation Skills
Quality Management
Chemistry
Vendors
Windows
Sales
Derivatives
Supply Chain Management
Petrochemical
Coatings
Minitab
Hazop
Pumps
Cross Functional Team Leadership
Design of Experiments
Capital Equipment
Developmental
Treatment
Procurement
Cmc
Cholesterol
Design
Feasibility Studies
Spc
Continuous Improvement
Materials Science
Keys
Feed
Powerpoint
Engineering Management
Lean Manufacturing
Ms Excel
Gmp
Hydrocarbon
Sugar
Engineers
Engineering
Usda
Process Control
Intermediates
Polymers
Control Software
Ms Project
Supply
Analytical Skills
Project Management
Product Development
Chemists
Process Engineering
Capital
R&D
Downstream Oil and Gas
Analysis
Process Simulation
Epc
Sap
Gas
Cross Functional Team
Project Engineering
Upstream
Chemical Engineering
Communication
Fmea
Modifications
Energy
Operators
Quality Assurance
Process Safety
Subject Matter Experts
Latex
Microsoft Access
Risk Assessment
Petroleum
Timelines
Nylon
Scopes
Certified Lean
Plants
Co2
Dmaic
Six Sigma
Pilot Plant
Food
Lotus Notes
Refining
Equipment Installation
Commissioning
Refinery
Green Belt
Process Improvement
Raw Materials
Technical Writing
Oracle
Fermentation
P&Id
Outlook
Equipment Selection
Pmbok
Billing
Factory
Analytical Skill
Manufacturing
Budgets
Formulation
Process Design
Equipment Design
Gas Processing
Commercialization
Process Optimization
Loraine Klein Photo 3

Loraine Klein

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Publications

Us Patents

Process For The Preparation Of 3,3-Dimethylbutanal

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US Patent:
6573409, Jun 3, 2003
Filed:
May 19, 2000
Appl. No.:
09/575107
Inventors:
Jerry R. Ebner - St. Charles MO
Zhi Guo - Chicago IL
Arnold Hershman - St. Louis MO
Loraine M. Klein - Streamwood IL
William D. McGhee - Fenton MO
Mark D. Paster - Chesterfield MO
Indra Prakash - Hoffman Estates IL
Assignee:
The Nutrasweet Company - Mt. Prospect IL
International Classification:
C07C 4500
US Classification:
568449, 568450, 568471, 568850
Abstract:
3,3-Dimethylbutanal is prepared from 3,3-dimethylbutanol. Intermediate 3,3-dimethylbutanol is obtained by reacting ethylene, isopropylene and sulfuric acid to produce a 3,3-dimethylbutyl ester which is hydrolyzed to the alcohol. The hvdrolysis step is effectively carried out by reactive distillation. Alternatively, 3,3-dimethylbutanal is prepared from 3,3-dimethylbutanol obtained by reduction of the corresponding carboxylic acid or 1,2-epoxy-3,3-dimethylbutane, or by hydrolysis of 1-halo-3,3-dimethylbutane. Fixed bed gas phase and stirred tank liquid phase processes are provided for converting 3,3-dimethylbutanol to 3,3-dimethylbutanal by catalytic dehydrogenation.

Process For The Preparation Of 3,3-Dimethylbutanal

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US Patent:
6803487, Oct 12, 2004
Filed:
May 29, 2003
Appl. No.:
10/447815
Inventors:
Jerry R. Ebner - St. Charles MO
Zhi Guo - Chicago IL
Arnold Hershman - St. Louis MO
Loraine M. Klein - Streamwood IL
William D. McGhee - Fenton MO
Mark Paster - Chesterfield MO
Indra Prakash - Hoffman Estates IL
Assignee:
The Nutrasweet Company - Mt. Prospect IL
International Classification:
C07C 4529
US Classification:
568449, 450471, 450840
Abstract:
3,3-Dimethylbutanal is prepared from 3,3-dimethylbutanol. Intermediate 3,3-dimethylbutanol is obtained by reacting ethylene, isopropylene and a mineral acid to produce a 3,3-dimethylbutyl ester which is hydrolyzed to the alcohol. The hydrolysis step is effectively carried out by reactive distillation. Alternatively, 3,3-dimethylbutanal is prepared from 3,3-dimethylbutanol obtained by reduction of the corresponding carboxylic acid or 1,2-epoxy-3,3-dimethylbutane, or by hydrolysis of 1-halo-3,3-dimethylbutane. Fixed bed gas phase and stirred tank liquid phase processes are provided for converting 3,3-dimethylbutanol to 3,3-dimethylbutanal by catalytic dehydrogenation.

Process For The Preparation Of 3,3-Dimethylbutanal

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US Patent:
7164049, Jan 16, 2007
Filed:
Mar 27, 2003
Appl. No.:
10/400558
Inventors:
Jerry R. Ebner - St. Charles MO, US
Zhi Guo - Chicago IL, US
Arnold Hershman - St. Louis MO, US
Loraine M. Klein - Streamwood IL, US
William D. McGhee - Fenton MO, US
Mark Paster - Chesterfield MO, US
Indra Prakash - Hoffman Estates IL, US
Assignee:
The Nutrasweet Company - Norwalk CT
International Classification:
C07C 27/00
US Classification:
568876, 568877
Abstract:
3,3-Dimethylbutanal is prepared from 3,3-dimethylbutanol. Intermediate 3,3-dimethylbutanol is obtained by reacting ethylene, isopropylene and a mineral acid to produce a 3,3-dimethylbutyl ester which is hydrolyzed to the alcohol. The hydrolysis step is effectively carried out by reactive distillation. Alternatively, 3,3-dimethylbutanal is prepared from 3,3-dimethylbutanol obtained by reduction of the corresponding carboxylic acid or 1,2-epoxy-3,3-dimethylbutane, or by hydrolysis of 1-halo-3,3-dimethylbutane. Fixed bed gas phase and stirred tank liquid phase processes are provided for converting 3,3-dimethylbutanol to 3,3-dimethylbutanal by catalytic dehydrogenation.

Process For The Preparation Of 3,3-Dimethylbutanal

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US Patent:
7348459, Mar 25, 2008
Filed:
Oct 24, 2006
Appl. No.:
11/552395
Inventors:
Jerry R. Ebner - St. Charles MO, US
Zhi Guo - Chicago IL, US
Arnold Hershman - St. Louis MO, US
Loraine M. Klein - Streamwood IL, US
William D. McGhee - Fenton MO, US
Mark D. Paster - Chesterfield MO, US
Indra Prakash - Hoffman Estates IL, US
Assignee:
The Nutrasweet Company - Mt. Prospect IL
International Classification:
C07C 45/29
US Classification:
568449, 568450
Abstract:
3,3-Dimethylbutanal is prepared from 3,3-dimethybutanol. Intermediate 3,3-dimethylbutanol is obtained by reacting ethylene, isopropylene and a mineral acid to produce a 3,3-dimethylbutyl ester which is hydrolyzed to the alcohol. The hydrolysis step is effectively carried out by reactive distillation. Alternatively, 3,3-dimethylbutanal is prepared from 3,3-dimethylbutanol obtained by reduction of the corresponding carboxylic acid or 1,2-epoxy-3,3-dimethylbutane, or by hydrolysis of 1-halo-3,3-dimethylbutane. Fixed bed gas phase and stirred tank liquid phase processes are provided for converted 3,3-dimethylbutanol to 3,3-dimethylbutanal by catalytic dehydrogenation.

Process For The Preparation Of Asparagine

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US Patent:
53269080, Jul 5, 1994
Filed:
Dec 9, 1992
Appl. No.:
7/988052
Inventors:
Robert Erickson - Des Plaines IL
Ron Bray - Buffalo Grove IL
Mark Johnson - Grayslake IL
Loraine Klein - Streamwood IL
Dennis A. Seagle - Buffalo Grove IL
International Classification:
C07C22900
US Classification:
562561
Abstract:
The present invention is an improved process for the synthesis of asparagine, a non-essential amino acid useful in food and medical applications. The process utilizes mineral acid to make an intermediate beta-methyl aspartate from a reaction mixture of aspartic acid and methanol. The intermediate product is then amminated in situ and asparagine collected with no need for an isolation step of the intermediates.

Preparation Of (S)-Decahydroisoquinoline-3-Carboxylic Acid T-Butylamide

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US Patent:
55874819, Dec 24, 1996
Filed:
Feb 20, 1996
Appl. No.:
8/603744
Inventors:
David R. Allen - Oak Brook IL
Scott Jenkins - San Francisco CA
Loraine Klein - Streamwood IL
Robert Erickson - Des Plaines IL
Diane Froen - Hoffman Estates IL
Assignee:
The Monsanto Company - St. Louis MO
International Classification:
C07D21716
US Classification:
546146
Abstract:
Methods for preparing (S)-N-tert-butyl-1,2,3,4-tetrahydro-3-isoquinoline-carboxamide ("tic-c"), and converting tic-c to (S)-decahydroisoquinoline-3-carboxylic acid t-butylamide ("tic-d") are disclosed. The initial step in the formation of tic-c involves the phosgenation of a substituted tetrahydroisoquinoline to form an N-carboxy anhydride. Tic-d is used as an intermediate in the synthesis of known compounds having pharmaceutical activity.
Loraine M Klein from Streamwood, IL, age ~66 Get Report