Bromine → 2-Bromo-1-(3,4-difluorophenyl)ethan-1-one

HRID 46555

반응식

HRID 46555 반응식
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([F:10])=[C:6]([F:11])[CH:5]=1)=[O:3].BrBr.ClC1C=C(Cl)C=CC=1C(=O)C[Br:19].C(C1C=CC=CC=1C(=O)CBr)C.C(C1C=CC(C(=O)CBr)=CC=1)(C)C.C(C1C=C(C=CC=1)C(=O)CBr)C(C)C.CC1C=C(C=CC=1C)C(=O)CBr.C(OC1C=C(C=CC=1)C(=O)CBr)C.C(OC1C=CC(C(=O)CBr)=CC=1)(C)C.C(OC1C=C(C=CC=1OCC)C(=O)CBr)C.FC1C=CC(F)=CC=1C(=O)CBr>C(Cl)(Cl)Cl.C(O)(=O)C>[F:11][C:6]1[CH:5]=[C:4]([CH:9]=[CH:8][C:7]=1[F:10])[C:2](=[O:3])[CH2:1][Br:19]

참가 물질

14

실험 절차

To a solution of 10.1 g. (0.065 mole) of 3,4-difluoroacetophenone in 100 ml. of glacial acetic acid was added 3.4 ml. (0.065 mole) of bromine dropwise. When the addition was complete the solution was stirred for 0.5 hr. and then stripped to dryness under reduced pressure. The residue was dissolved in chloroform and washed with aqueous sodium bicarbonate. Evaporation of the organic phase provided 14.8 g. (97%) of colorless liquid product. Similarly prepared were 2,4-dichlorophenacyl bromide, o-ethylphenacyl bromide, p-isopropylphenacyl bromide, m-isobutylphenacyl bromide, 3,4-dimethylphenacyl bromide, m-ethoxyphenacyl bromide, p-isopropoxyphenacyl bromide, 3,4-diethoxyphenacyl bromide, and 2,5-difluorophenacyl bromide.

후처리

  1. additionWhen the addition
  2. washwashed with aqueous sodium bicarbonate
  3. customEvaporation of the organic phase
  4. customprovided 14.8 g
  5. customSimilarly prepared

출처 및 근거

ORD 기록
ord-51ac15fa7aa84ece864078149c112857
출처 데이터셋
uspto-grants-1979_11
특허 번호
US04173650

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