تفاعل #9728

ord-a1c31f05a7504c58b2c582a15b337fab

معادلة التفاعل

c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCOC(=O)/C=C/c1ccc(CO)cc1C
ethyl(2E)-3-[4-(hydroxymethyl)-2-methylphenyl]prop-2-enoate
CCOC(=O)/C=C/c1ccc(CO)cc1C
intermediate 19
CCOC(=O)/C=C/c1ccc(CO)cc1C
ethyl(2E)-3-[4-(hydroxymethyl)-2-methylphenyl]prop-2-enoate
ClCCl.O
dichloromethane water
BrC(Br)(Br)Br
carbon tetrabromide
CCOC(=O)/C=C/c1ccc(CBr)cc1C
title compound
CCOC(=O)/C=C/c1ccc(CBr)cc1C
Ethyl(2E)-3-[4-(bromomethyl)-2-methylphenyl]prop-2-enoate

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe organic phase separated
  2. 2
    غسيلwashed with more water, brine
  3. 3
    تجفيفdried over sodium sulfate
  4. 4
    أخرىthen evaporated in vacuo
  5. 5
    أخرىThe isolated product was further purified by flash column chromatography

الإجراء التجريبي

A solution of ethyl(2E)-3-[4-(hydroxymethyl)-2-methylphenyl]prop-2-enoate (intermediate 19, 1.389 g) in dry dichloromethane (40 ml) was cooled to 0° C. and treated with carbon tetrabromide (2.3 g) followed by, in small portions, triphenylphosphine (1.82 g). The resulting solution was stirred thus overnight, then poured into dichloromethane/water and the organic phase separated and washed with more water, brine and dried over sodium sulfate then evaporated in vacuo. The isolated product was further purified by flash column chromatography using cyclohexane:ethyl acetate (9:1) as an eluent which gave the title compound as a white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091237B2uspto-grants-2006_08