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. a-Fluoro- and a,a-difluoroalkanals by substitution of vicinal bromofluoroalkanes and subsequent Pummerer rearrangement
 
research article

a-Fluoro- and a,a-difluoroalkanals by substitution of vicinal bromofluoroalkanes and subsequent Pummerer rearrangement

Suga, Hiroaki
•
Schlosser, Manfred  
1990
Tetrahedron

2-Fluoro- or 2,2-difluoro-1-bromoalkanes readily undergo nucleophilic substitution by sodium thiophenolate to give 2-fluoro- or 2,2-difluoroalkyl Ph sulfides. The latter can be oxidized to the corresponding sulfoxides. Heating with acetic anhydride produces 2-fluoro- and 2,2-difluoro-1-(phenylthio)alkyl acetates, which can then be cleaved to give 2-fluoro- and 2,2-difluoro-1-(phenylthio)-1-alkanols or the 2-fluoro- and 2,2-difluoroalkanals if not reduced to give 2-fluoro- or 2,2-difluoro-1-alkanols. [on SciFinder (R)]

  • Details
  • Metrics
Type
research article
DOI
10.1016/S0040-4020(01)86763-6
Author(s)
Suga, Hiroaki
•
Schlosser, Manfred  
Date Issued

1990

Published in
Tetrahedron
Volume

46

Issue

12

Start page

4261

End page

4264

Subjects

Substitution reaction (of bromofluoroalkanes with thiophenoxide); Pummerer reaction (of fluoro sulfoxides); Aldehydes Role: SPN (Synthetic preparation)

•

PREP (Preparation) (fluoro

•

prepn. of

•

from bromofluoroalkanes)

•

alkanal fluorinated; substitution bromofluoroalkane thiophenoxide; Pummerer rearrangement fluoro sulfoxide

Note

CAN 113:171600

25-15

Benzene, Its Derivatives, and Condensed Benzenoid Compounds

Inst. Chim. Org.,Univ. Lausanne,Lausanne,Switz.

Journal

written in English.

129973-39-3P; 129973-40-6P; 129973-41-7P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and Pummerer rearrangement of); 129973-48-4P; 129973-49-5P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. and conversion to aldehyde); 100655-82-1P; 129973-37-1P; 129973-38-2P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and oxidn. of); 129973-43-9P; 129973-44-0P; 129973-45-1P; 129973-53-1P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and redn. of); 129660-35-1P; 129973-42-8P; 129973-46-2P; 129973-47-3P; 129973-50-8P; 129973-51-9P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of); 930-69-8 (Sodium thiophenoxide) Role: RCT (Reactant), RACT (Reactant or reagent) (substitution reaction of, with bromofluoroalkanes); 1786-34-1; 108661-89-8; 129973-52-0 Role: RCT (Reactant), RACT (Reactant or reagent) (substitution reaction of, with thiophenoxide)

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/20.500.14299/226867
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