Reacción #969849

ord-b2d7178f7d184b7fa035b61e63a2c1cf

Ecuación de reacción

[N-]=[N+]=[N-].[Na+]
NaN3
COC(=O)/C=C/CBr
methyl 4-bromocrotonate
COC(=O)/C=C/CN=[N+]=[N-]
title product
Rendimiento 80.1%
COC(=O)/C=C/CN=[N+]=[N-]
(E)-Methyl 4-azidobut-2-enoate
Rendimiento 80.1%

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Temperatura
-20°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe mixture was stirred at 0° C. for 4 h
  2. 2
    Otroevaporated
  3. 3
    Filtraciónfiltered
  4. 4
    Otroevaporated
  5. 5
    Otrochromatographic purification on SiO2 column
  6. 6
    Lavadoeluted with EtAc/Hexane (1:25 to 1:10)

Procedimiento

To the solution of NaN3 (2.80 g, 43.01 mmol) in 100 ml of DMF at −20° C. was added methyl 4-bromocrotonate (5.00 ml, 85%, 36.10 mmol). After stirred at −20° C. for 30 min, the mixture was stirred at 0° C. for 4 h, evaporated, suspended with EtAc/Hexane (1:1), filtered, evaporated and chromatographic purification on SiO2 column eluted with EtAc/Hexane (1:25 to 1:10) to afford HRMS for 4.08 g (80%) of the title product. 1H NMR (CDCl3) 6.88 (m, 1H), 6.06 (ddd, 1H, J−=1.7, 3.4, 15.6 Hz), 3.97 (dd, 2H, J=1.2, 4.96 Hz), 3.73 (s, 3H); 13C NMR 166.23, 140.86, 123.49, 51.95, 51.36; ESI MS m/z+ 182.5 (M+Na+H2O); HRMS m/z+ (C5H7N3O2+H2O+Na) calcd 182.0542, found 182.0548.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08236319B2uspto-grants-2012_08