BSC SEM : IV Unit : VI (Organic Synthesis Via Enolates)

BSC SEM : IV Unit : VI (Organic Synthesis Via Enolates)

Faculty : Science Department : Chemistry Course : BSC SEM : IV Unit : VI (organic synthesis via enolates) Paper : II Teacher : Dr M Karunakar Topic brief description: EAA, ME –synthesis and their chemical properties ORGANIC SYNTHESIS VIA ENOLATES: ACTIVE METHYLENE COMPOUNDS O O- -CH2-EWG -CH C CH C α- hydrogens always in acidic nature α Base can abstract these protane to form a carbanion Active methylene group Enolate (stable) Enolate = anion of enol Active methylene group Enolates are imp compds in org. synthesis for new C-C bond formation EWG EWG Carbonyl β α Ester α -Active methylene carban Ethyl Aceto Acetate (EAA) Acetyl Aceto Ester (AAE) β- keto ester imp β- keto ester Base abstract proton from ketone methyl group carbanion which generated attack upon ester carbonyl carbon H- transferred to O- Cyclo addition Ketene 2 moles EAA H Enol form Important Enol of EAA v Important 2 moles Enol and keto form of EAA Pyrogallol OR Important 1,2,3-trihydroxy benzene Enol of EAA Vii Viii iX α α α R-X Mono alkylation -------> dialkyl In this case act as strong base, alkyl halide undergo elimination Mono Acyl------------ Di acyl substituted Key thing to remember always in conversion important EAA Easy to remember imp H shifted OH H Easy to remember Applications 1. Synthesis of methyl ketones. Example: 2-butanone., 3-methyl-2-pentanone 2. Synthesis of 1, 3 di ketone(β-diketone) example: 2,4-pentanone Ketonic 1,4 diketone (γ -diketone) example: 2,5-hexadione hydrolysis 3.Synthesis carboxylic acid , mono alkyl substituted carboxylic acid, di carboxylic acid [succinic acid, glutaric acid, Adipic acid} , highter carboxylic acid 4. Synthesis of γ-Keto acid Acidic hydrolysis 5. Synthesis of α,β-unsaturated acid eg :crotonic acid hydrolysis Note: in ketonic hydrolysis(dilute Aqueos alkali /acid): prouct formed is methyl ketone derivative in acidic hydrolysis ( Concentrated ethanolic aloholic KOH sol)produce acetic acid and its derivatives Application of EAA R = alkyl gp 1. Synthesis of Methyl Ketone *Mainly depends on R-X Q: how will you synthesize 2- butanone(methyl ethyl ketone) from EAA …………………………………… 2-pentanone( methyl propyl ketone) ………. important 2- 2- butanone or Methyl ethyl ketone or 2,4-pentanone(1, 3 di ketone/ β-diketone) 1 2 3 4 5 1 Carbanion of EAA I-I imp How can be synthesize butyric acid from EAA imp How can be synthesize 2-methyl pentanoic acid from EAA Succnic acid α chloro ester H Di iodo alkane 2moles of EAA with 2 moles of base + di iodo alkane important Di iodo methane Glutaric acid(5C) Adipic acid(6C) Q: How can be syntheise Succinic acid, methyl substituted succinic acid, glutaric acid, adipic acid fromEAA β α γ Synthesis of α,β-unsaturated acid/ crotonic acid Acetaldehyde + EAA Or M E -COOH COOC2H5 α-halogenation α-Alkylation Mono alkyl di alkyl hydrolysis .

View Full Text

Details

  • File Type
    pdf
  • Upload Time
    -
  • Content Languages
    English
  • Upload User
    Anonymous/Not logged-in
  • File Pages
    39 Page
  • File Size
    -

Download

Channel Download Status
Express Download Enable

Copyright

We respect the copyrights and intellectual property rights of all users. All uploaded documents are either original works of the uploader or authorized works of the rightful owners.

  • Not to be reproduced or distributed without explicit permission.
  • Not used for commercial purposes outside of approved use cases.
  • Not used to infringe on the rights of the original creators.
  • If you believe any content infringes your copyright, please contact us immediately.

Support

For help with questions, suggestions, or problems, please contact us