photo of Dr. Lynn Anderson

A. Lynn Anderson

Senior Lecturer

Office: 368 Greenquist

Telephone: (262) 595-2633

Fax : (262) 595-2056

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Courses Typically Taught
 
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Organic Laboratory 323, Chemistry 115, 215, Lecture and Lab

Education

Experience

 

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Publications and Patents

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Professional Associations

Research Interests and Objectives

PAST

During my employment at Sinclair Research, Inc. I studied the hydrochlorination of alkenes, acid and base catalyzed condensations, and alkene absorption in sulfuric acid.

While a senior research chemist at Michigan Chemical, I worked primarily on the synthesis of novel organic halogen compounds for use as flame retardants. The work led to the issuance of over 60 United States Patents and eventually to the commercialization of two products. A major success was the discovery of a flame retardant additive now manufactured under the trade name FF-680. This compound is accepted by the plastics industry as a non-toxic, environmentally acceptable replacement for the polybrominated biphenyls formerly used.

During the course of my employment in Michigan, I coordinated efforts with applications chemists/engineers on structure-property relationship studies for polymer additives. I developed industrial processes for flame retardants using the Williamson ether synthesis. Additional studies were performed for phase transfer catalysis assisted synthetic routes to flame retardants and herbicide intermediates. Halogenated telomers were suggested and studied as polymer modifiers. Exploratory research was conducted on unique halogenated intumescent compounds for potential civilian/military uses.

As a group leader at Stepan Chemical, I and members of my group conducted syntheses of flavor and fragrance compounds, feasibility studies of novel synthetic routes to surfactants, and the preparation of aldehydes via oxidation.

PRESENT

Since beginning my own consultancy, I have been involved in a wide array of projects. Significant projects include the following:

FUTURE

My plans for future work lie in three main areas.

1. Nucleophilic Substitution Reactions: For over twenty years I have maintained an on-going interest in this generalized reaction. The Williamson ether synthesis and metal hydride reactions, typically very efficient, have historically proven to be effective tools in organic synthesis. I intend to investigate further applications of these and other nucleophilic substitution reactions in the synthesis of highly symmetrical compounds.

2. Organic Halogen Compounds: Organic bromine and chlorine compounds, because of their accessibility, outnumber the corresponding fluorine and iodine analogs. Organobromine and chlorine compounds have very similar chemistry; in many cases the extremes of fluorine and iodine substitution give rise to unique chemistries. My intentions are to investigate this aspect of halogen chemistry in more detail.

3. N For One Synthesis: An ideal chemical process is one in which each molecule entering a chemical process exits as a useful new molecule. I wish to investigate synthetic routes with the potential of giving N =2,3,... useful molecules per reaction.

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