Reacción #87964

ord-6d56a827b0c04ac2a2287ec46d1153ea

Ecuación de reacción

CC(C)(Br)Br
dibromopropane
[Cl-].[Na+]
sodium chloride
Cl
HCl
CC(C)[N-]C(C)C.[Li+]
LDA
[Cl-].[NH4+]
ammonium chloride
O=C(O)c1cccs1
thienoic acid
O=C(O)c1ccc(CCCBr)s1
title compound
Rendimiento 123.5%
O=C(O)c1ccc(CCCBr)s1
5-(3-bromopropyl)thiophene-2-carboxylic acid
Rendimiento 123.5%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGwas stirred for 3 days
  2. 2
    ExtracciónThe organic material was extracted with ethyl acetate
  3. 3
    Secadothe organic layer was dried over sodium sulfate
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated

Procedimiento

To a solution consisting of thienoic acid (10 g, 78 mmol) in THF (150 mL) at −78° C. was added an LDA solution (85 mL, 170 mmol, 2 M in heptanes/THF/ethylbenzene, Sigma-Aldrich) dropwise over 20 minutes, and the reaction mixture was stirred 40 minutes. To the reaction mixture was then added dibromopropane (23.8 g, 117 mmol) in one portion, and the reaction mixture was allowed to warm to room temperature and was stirred for 3 days. To the reaction mixture was added 50 mL each of a saturated aqueous solution of ammonium chloride, a saturated aqueous solution of sodium chloride, and 6 N HCl. The organic material was extracted with ethyl acetate and the organic layer was dried over sodium sulfate, filtered, and concentrated to afford the title compound as a yellow oil (24.0 g). The product was used without further purification; TLC Rf 0.5 (solvent system: 30:70:1 v/v ethyl acetate-hexanes-acetic acid).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09440919B2uspto-grants-2016_09