Reacción #77782

ord-f7a7d38a65524aa78f0024818bae38cd

Ecuación de reacción

Brc1ccc2c(c1)CCN2
5-bromo-indoline
CC(C)(C)OC(=O)OC(=O)[O-]
tert.-butyldicarbonate
CC(C)(C)OC(=O)N1CCc2cc(Br)ccc21
5-Bromo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester
Rendimiento 89.0%

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction mixture was concentrated in vacuo
  2. 2
    Otrotriturated with hexane

Procedimiento

4 g (20 mmol) 5-bromo-indoline in 50 ml CH2Cl2 were treated with 4.4 g (20 MMOL) di.-tert.-butyldicarbonate at RT over night. The reaction mixture was concentrated in vacuo and triturated with hexane to yield 5.3 g (89%) 5-Bromo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester as colorless solid, MS: 297 (M, 1Br).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06706751B2uspto-grants-2004_03