Repository logo

Infoscience

  • English
  • French
Log In
Logo EPFL, École polytechnique fédérale de Lausanne

Infoscience

  • English
  • French
Log In
  1. Home
  2. Academic and Research Output
  3. Journal articles
  4. 1- and 2-fluoroalkyl carboxylates
 
research article

1- and 2-fluoroalkyl carboxylates

Limat, Dominique
•
Guggisberg, Yves
•
Schlosser, Manfred  
1995
Liebigs Annalen

The 2-fluoroalkyl esters, e.g. FCH2CH2CO2Me are readily accessible by the base-catalyzed acylation of fluorohydrines. A two-step procedure is required to prep. the 1-fluoroalkyl esters: conversion of alk-1-enyl carboxylates ("ene esters") into the 2-bromo-1-fluoroalkyl esters by simultaneous treatment with N-bromosuccinimide and HF followed by the reductive replacement of bromine by tributyltin hydride. Alka-1,3-dienyl carboxylates ("diene esters") undergo 1,4-addn. of bromine and fluorine. The resulting 4-bromo-1-fluoralk-2-enyl carboxylates undergo a substitution reaction with sodium benzenesulfinate to afford the sulfones or oxidn. with DMSO to yield the 4-oxo derivs. 2-Fluoroethanol was added to NaH followed by AcOH to give 2-fluoroacetate. 2-Bromo-1-fluoroethyl acetate (prepn. given) and Bu3SnH were kept at 90 Deg for 1 h to give 1-fluoroethyl acetate. [on SciFinder (R)]

  • Details
  • Metrics
Type
research article
DOI
10.1002/jlac.1995199505123
Author(s)
Limat, Dominique
•
Guggisberg, Yves
•
Schlosser, Manfred  
Date Issued

1995

Published in
Liebigs Annalen
Issue

5

Start page

849

End page

53

Subjects

fluoroalkyl carboxylate; ene ester; diene ester; organofluorine compd

Note

CAN 123:111530 23-17 Aliphatic Compounds Inst. Chim. org.,Univ. Lausanne,Lausanne-Dorigny,Switz. Journal 0947-3440 written in English. 108-05-4 (Vinyl acetate); 371-62-0 (2-Fluoroethanol); 693-38-9 (Vinyl palmitate); 1813-13-4; 3109-99-7; 17574-85-5; 17574-86-6; 35694-19-0; 35694-20-3; 52062-24-5; 52062-25-6; 74322-79-5; 110500-35-1; 150020-39-6; 165614-45-9; 165614-46-0; 165614-47-1; 165614-48-2; 165614-49-3; 165614-50-6; 165614-51-7; 165614-52-8; 165614-53-9; 165614-54-0 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of fluoroalkyl carboxylates); 165614-20-0P; 165614-21-1P; 165614-22-2P; 165614-23-3P; 165614-24-4P; 165614-25-5P; 165614-26-6P; 165614-27-7P; 165614-28-8P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of fluoroalkyl carboxylates); 462-26-0P; 1786-46-5P; 137555-31-8P; 165614-09-5P; 165614-10-8P; 165614-11-9P; 165614-12-0P; 165614-13-1P; 165614-14-2P; 165614-15-3P; 165614-16-4P; 165614-17-5P; 165614-18-6P; 165614-19-7P; 165614-29-9P; 165614-30-2P; 165614-31-3P; 165614-32-4P; 165614-33-5P; 165614-34-6P; 165614-35-7P; 165614-36-8P; 165614-37-9P; 165614-38-0P; 165614-39-1P; 165614-40-4P; 165614-41-5P; 165614-42-6P; 165614-43-7P; 165614-44-8P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of fluoroalkyl carboxylates)

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCO  
Available on Infoscience
March 3, 2006
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/226919
Logo EPFL, École polytechnique fédérale de Lausanne
  • Contact
  • infoscience@epfl.ch

  • Follow us on Facebook
  • Follow us on Instagram
  • Follow us on LinkedIn
  • Follow us on X
  • Follow us on Youtube
AccessibilityLegal noticePrivacy policyCookie settingsEnd User AgreementGet helpFeedback

Infoscience is a service managed and provided by the Library and IT Services of EPFL. © EPFL, tous droits réservés