5-Phenylpent-4-enyl-1-ol → HCID 11105652, 화합물

HRID 1856437

반응식

HRID 1856437 반응식
[C:1]1(/[CH:7]=[CH:8]/[CH2:9][CH2:10][CH2:11][OH:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>ClC1CCCOC1C1C=CC=CC=1>[C:1]1(/[CH:7]=[CH:8]/[CH2:9][CH2:10][CH:11]=[O:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

참가 물질

3

실험 절차

To a dry 3 liter 3-necked flask equipped with mechanical stirrer, thermometer and nitrogen inlet was added 1.5 liter of dry dichloromethane (a) and 95 g of dry pyridine (b). The stirred solution was cooled ot an internal temperature of 5° and 60 g of chromium trioxide (c) was added in one portion. The mixture was stirred an additional 5 minutes and then allowed to warm to 20° over 60 minutes, giving a solution of Collins reagent. A solution of 16.2 g of trans-5-phenyl-4-penten-1-ol (d) in 100 ml of dry dichloromethane (e) was then added rapidly. The mixture was stirred an additional 15 minutes and then decanted from the residue. The residue, a black tar, was washed with ether (3×500 ml) and the combined organic solution was worked up in the usual manner. Evaporation of the solvent gave the aldehyde (15 g) as a pale yellow liquid. TLC; silica gel HF254 ; ethyl acetate/benzene 1:9 Rf 0.50.

후처리

  1. customdecanted from the residue
  2. washThe residue, a black tar, was washed with ether (3×500 ml)
  3. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-d2f324a05edf4ee8a360def3aa80df96
출처 데이터셋
uspto-grants-1980_08
특허 번호
US04219489

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