Reacción #1702105

ord-f1e890d60c44408586cd225a88eb3883

Ecuación de reacción

CC1=CC[C@@H](C(=O)O)CC1
(1S)-4-Methyl-cyclohex-3-ene-1-carboxylic acid
Cc1ccccc1
toluene
O=C(Cl)C(=O)Cl
oxalyl chloride
CC1=CC[C@@H](C(=O)Cl)CC1
(1S)-4-methyl-cyclohex-3-ene-1-carboxylic acid chloride

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturato warm to ambient temperature
  2. 2
    ConcentraciónThe solution was concentrated
  3. 3
    workup.ADDITIONtreated with hexanes
  4. 4
    Concentraciónconcentrated again

Procedimiento

(1S)-4-Methyl-cyclohex-3-ene-1-carboxylic acid (250 mg, 1.78 mmol), azeotropically dried by evaporation from toluene was dissolved in dichloromethane (4 mL) and treated with dimethylformamide (1 drop). The reaction mixture was cooled to 0° C. and treated dropwise with oxalyl chloride (0.42 mL, 4.5 mmol). The reaction mixture was allowed to warm to ambient temperature while stirring for 4 h. The solution was concentrated, treated with hexanes and concentrated again to afford (1S)-4-methyl-cyclohex-3-ene-1-carboxylic acid chloride as a light yellow oil which was used immediately in the next step.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08765722B2uspto-grants-2014_07