تفاعل #52356

ord-e5b160fb9bce42f88443af06854a81fe

معادلة التفاعل

CC1(C)CN(C2CC2)Cc2ccc(C=O)cc21
Intermediate 25
CC1(C)CN(C2CC2)Cc2ccc(C=O)cc21
2-cyclopropyl-4,4-dimethyl-1,2,3,4-tetrahydroisoquinoline-6-carboxaldehyde
BrC(Br)(Br)Br
carbon tetrabromide
CC1(C)CN(C2CC2)Cc2ccc(C=O)cc21
2-cyclopropyl-4,4-dimethyl-1,2,3,4-tetrahydroisoquinoline-6-carboxaldehyde
CCOC(C)=O
ethyl acetate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenyl phosphine
CC1(C)CN(C2CC2)Cc2ccc(C=C(Br)Br)cc21
title compound
CC1(C)CN(C2CC2)Cc2ccc(C=C(Br)Br)cc21
6-(2,2-Dibromo-vinyl)-2-cyclopropyl-4,4-dimethyl-1,2,3,4-tetrahydroisoquinoline

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITAfter 1.5 h between 0° C. and 10° C.

الإجراء التجريبي

A stirred, cooled (ice-bath) solution of triphenyl phosphine (0.53 g, 2 mmol) in anhydrous dichloromethane was treated with carbon tetrabromide (0.35 g, 1 mmol) under argon. After 0.5 h, a solution of 2-cyclopropyl-4,4-dimethyl-1,2,3,4-tetrahydroisoquinoline-6-carboxaldehyde (Intermediate 25, 0.13 g, 0.57 mmol) in dichloromethane (2 mL) was cannulated into the reaction mixture. After 1.5 h between 0° C. and 10° C., the reaction mixture was subjected to flash column chromatography over silica gel (230-400 mesh) using 3-5% ethyl acetate in hexane as the eluent to afford the title compound as a viscous, pale yellow oil (0.18 g, 82%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06855512B2uspto-grants-2005_02