Carbon tetrabromide → Ethyl 2-[4-(bromomethyl)phenoxy]acetate

HRID 1459434노트

반응식

HRID 1459434 반응식
O[CH2:2][C:3]1[CH:15]=[CH:14][C:6]([O:7][CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:5][CH:4]=1.C(Br)(Br)(Br)[Br:17].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(Cl)Cl>[Br:17][CH2:2][C:3]1[CH:15]=[CH:14][C:6]([O:7][CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:5][CH:4]=1

참가 물질

5

반응물 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 11413157Acetic acid, [4-(hydroxymethyl)phenoxy]-, ethyl ester

생성물 1

HCID 12870369Ethyl 2-[4-(bromomethyl)phenoxy]acetate수율 74.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a 1 L round bottomed flask with a stirring bar, addition funnel and an argon inlet was added ethyl 2-(4-hydroxymethylphenoxy)acetate 35-4 (7.47 g, 35.53 mmol), CBr4 (13.26 g, 39.97 mmol) and dry CH2Cl2 (300 mL). This solution was cooled in an ice bath and and a solution of triphenyl phosphine (10.48 g, 39.97 mmol) in CH2Cl2 (100 mL) was added dropwise over 1 h. The ice bath was allowed to expire and and the mixture was stirred at ambient temperature 18 h. The solvent was removed in vacuo and the residue was chromatographed directly on 200 g of silica gel useing 15% EtOAc-hexane as eluant. There was obtained ethyl 2-(4-bromomethylphenoxy)acetate 35-5 (7.2 g, 74%) as a low melting solid, mp.: 44°-45° C. 1H NMR (CDCl3): δ 1.29 (t, J=7 Hz, 3H), 4.26 (q, J=7 Hz, 2H), 4.48 (s, 2H), 4.61 (s, 2H), 6.86 (d, J=9 Hz, 2H), 7.32 (d, J=9HZ, 2H).

후처리

  1. additionTo a 1 L round bottomed flask with a stirring bar, addition funnel and an argon inlet
  2. temperatureThis solution was cooled in an ice bath
  3. customThe solvent was removed in vacuo
  4. customthe residue was chromatographed directly on 200 g of silica gel useing 15% EtOAc-hexane as eluant

출처 및 근거

ORD 기록
ord-0e09a5f283984d4ab65d8843efe6c82e
출처 데이터셋
uspto-grants-1998_12
특허 번호
US05854245

반응 노트

불러오는 중…