Reaktion #969855

ord-ba6cdf2b3bb44480aa7b805b882d90d0

Reaktionsgleichung

CCOC(=O)/C=C\C#N
(Z)-ethyl 3-cyanoacrylate
O=C(O)Cc1cccs1
thiol acetic acid
CCN(C(C)C)C(C)C
DIPEA
C1CCOC1
THF
C1CCOC1
THF
CCOC(=O)CC(C#N)SC(C)=O
title compound
Ausbeute 65.0%
CCOC(=O)CC(C#N)SC(C)=O
Ethyl 3-(acetylthio)-3-cyanopropanoate
Ausbeute 65.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeroom temperature overnight
  2. 2
    EinengenThe mixture was concentrated
  3. 3
    workup.ADDITIONdiluted with CH2Cl2
  4. 4
    Waschenwashed with saturated NaHCO3
  5. 5
    Trocknendried over MgSO4
  6. 6
    Filtrationfiltered
  7. 7
    Sonstigeevaporated
  8. 8
    Sonstigepurified by SiO2 chromatography (1:4 EtAC/Hexane)

Vorschrift

(Z)-ethyl 3-cyanoacrylate (5.01 g, 40.00 mmol) in 80 ml of THF at −20° C. was added the solution of thiol acetic acid (5.0 ml, 70.15 mmol) and DIPEA (16.0 ml, 92.03 mmol) in 20 ml of THF in 30 min. The reaction was kept at −20° C. for 4 hr then room temperature overnight. The mixture was concentrated, diluted with CH2Cl2, washed with saturated NaHCO3, dried over MgSO4, filtered, evaporated and purified by SiO2 chromatography (1:4 EtAC/Hexane) to afford 5.22 g (65%) of the title compound. Rf=0.25 (1:4 EtAC/Hexane); 1H NMR (CDCl3), 4.44 (m, 1H), 4.11 (dd, 2H, J=7.1, 14.3 Hz), 3.38 (m, 1H), 3.15 (m, 1H), 2.17 (s, 3H), 1.19 (t, 3H, J=7.2 Hz); 13C NMR 194.12, 173.21, 119.82, 61.35, 33.52, 30.08, 14.62; MS m/z+ 225.9 (MW+Na), m/z− 201.7 (MW−H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08236319B2uspto-grants-2012_08