Organic Synthesis-B - कार्बनिक संश्लेषण - ख – Adv

Program/Class:

Degree/ Bachelor

of Science

Year: Third

Semester: Sixth

Subject: Chemistry

Course Title: Organic Synthesis B

Course Learning Outcomes

This paper provides detailed knowledge of synthesis of various class of organic compounds and functional groups inter conversion. Organic synthesis is the most important branch of organic chemistry which provides jobs in production & QC departments related to chemicals, drugs, medicines, FMCG etc. industries. The study of natural products and heterocyclic compounds offers an excellent strategy toward identifying novel biological probes for a number of diseases. Historically, natural products have played an important role in the development of pharmaceutical drugs for a number of diseases including cancer and infection.

∙ It relates and gives an analytical aptitude for synthesizing various industrially important

compounds. ∙ Learn the different types of alkaloids, & terpenes etc and their chemistry and

medicinal importance. ∙ Explain the importance of natural compounds as lead molecules for new drug discovery.

Credits: 4

Core Compulsory

Max. Marks: –25+75

Min. Passing Marks: 40

Unit

Topics

I

Reagents in Organic Synthesis

A detailed study of the following reagents in organic transformations

Oxidation with DDQ, CAN and SeO2, mCPBA, Jones Oxidation, PCC, PDC, PFC, Collin’s reagent and ruthenium tetraoxide. Reduction with NaBH4, LiAlH4, Meerwein-Ponndorf-Verley (MPV) reduction, Wilkinson’s catalyst, Birch reduction, DIBAL-H

II

Organometallic Compounds-Organomagnesium compounds: the Grignard reagents, formation, structure and chemical reactions. Organozinc compounds: formation and chemical reactions. Organolithium compounds: formation and chemical reactions.

III

Chemistry of Aldehydes and ketones: Nomenclature and structure of the carbonyl groups, synthesis of aldehydes and ketones with particular reference to the synthesis of aldehydes from acid chlorides, synthesis of aldehydes and ketones uses 1, 3-dithianes, synthesis of ketones from nitrites and from carboxylic acids, Physical properties. Mechanism of nucleophillic additions to carbonyl group with particular emphasis on benzoin, aldol, Perkin and Knoevenagel condensations, Condensation with ammonia and its derivatives. Wittig reaction, Mannich reaction. Oxidation of aldehydes, Cannizzaro reaction, MPV, Clemmensen, Wolff-Kishner, LiAlH4 and NaBH4 reductions. Halogenation of enolizable ketones An introduction to α, β unsaturated aldehydes and Ketones

IV

Carboxylic acids and their Functional Derivatives

Nomenclature and classification of aliphatic and aromatic carboxylic acids. Preparation and reactions. Acidity (effect of substituents on acidity) and salt formation, Reactions: Mechanism of reduction, substitution in alkyl or aryl group. Preparation and properties of dicarboxylic acids such as oxalic, malonic, succinic, glutaric, adipic and phthalic acids and unsaturated carboxylic acids such as acrylic, crotonic and cinnamic acids, Reactions: Action of heat on hydroxy and amino acids, and saturated dicarboxylic acids, stereospecific addition to maleic and fumaric acids. Preparation and reactions of acid chlorides, acid anhydrides, amides and esters, acid and alkaline hydrolysis of esters, trans-esterification.

V

Organic Synthesis via Enolates

Acidity of α-hydrogens, alkylation of diethyl malonate and ethyl acetoacetate, Synthesis of ethyl acetoacetate: the Claisen condensation, Keto-enol tautomerism of ethyl acetoacetate. Alkylation of 1, 3-dithianes, Alkylation and acylation of enamines.

VI

Organic Compounds of Nitrogen- Preparation of nitroalkanes and nitroarenes, Chemical reactions of nitroalkanes. Mechanisms of nucleophilic substitution in nitroarenes and their reductions in acidic, neutral and alkaline media, Picric acid. Halonitroarenes: reactivity, Structure and nomenclature of amines, physical properties, Stereochemistry of amines, Separation of a mixture of primary, secondary and tertiary amines. Structural features effecting basicity of amines. Amine salts as phase-transfer catalysts, Preparation of alkyl and aryl amines (reduction of nitro compounds, nitrities), reductive amination of aldehydic and ketonic compounds, Gabriel phthalimide reaction, Hofmann bromamide reaction. Reactions of amines, electrophilic aromatic substituton in aryl amines, reactions of amines with nitrous acid. Synthetic transformations of aryl diazonium salts, azo coupling

VII

Heterocyclic Chemistry

Molecular orbital picture and aromatic characteristics of pyrrole, furan, thiophene and pyridine, Methods of synthesis and chemical reactions with particular emphasis on the mechanism of electrophilic substitution, Mechanism of nucleophilic substitution reaction in pyridine derivatives, Comparison of basicity of pyridine, piperidine and pyrrole. Introduction to condensed five and six membered heterocycles, Preparation and reactions of indole, quinoline and isoquinoline with special reference to Fisher indole synthesis, Skraup synthesis and Bischler-Nepieralski synthesis, Mechanism of electrophilc substitution reactions of indole, quinoline and isoquinoline

VIII

Natural Products

Alkaloids & Terpenes: Natural occurrence, General structural features, their physiological action, Hoffmann’s exhaustive methylation, Emde’s modification;. Medicinal importance of Nicotine, Hygrine, Quinine, Morphine, Cocaine, and Reserpine. Natural Occurrence and classification of terpenes, isoprene rule