Water → 3-Bromobenzo[b]thiophene-5-carboxaldehyde

HRID 581725노트

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HRID 581725 반응식
[S:1]1[CH:5]=[CH:4][C:3]2[CH:6]=[C:7]([CH:10]=[O:11])[CH:8]=[CH:9][C:2]1=2.[Br:12]Br.O.C(OCC)(=O)C>C(O)(=O)C>[Br:12][C:4]1[C:3]2[CH:6]=[C:7]([CH:10]=[O:11])[CH:8]=[CH:9][C:2]=2[S:1][CH:5]=1

참가 물질

6

실험 절차

To a solution of 3 g of benzo[b]thiophene-5-carbaldehyde in 30 ml of acetic acid is dropwise added 1.43 ml of bromine with ice-cooling. The temperature of the reaction mixture is elevated to room temperature, at which temperature the mixture is stirred for three hours. After the reaction, 50 ml of water and 50 ml of ethyl acetate are added to the thus stirred reaction mixture, and the resulting organic layer was separated, washed successively with water, a saturated aqueous sodium hydrogencarbonate solution and a saturated saline solution and then dried over anhydrous magnesium sulfate. Thereafter, the solvent is removed from the thus dried layer by distillation under reduced pressure. The residue obtained is purified by a moderate pressure column chromatography [eluent:hexane:ethyl acetate=20:1], to obtain 4.2 g of 3-bromobenzo[b]thiophene-5-carbaldehyde.

후처리

  1. temperaturecooling
  2. customis elevated to room temperature, at which temperature
  3. additionare added to the thus stirred reaction mixture
  4. customthe resulting organic layer was separated
  5. washwashed successively with water
  6. dry with materiala saturated aqueous sodium hydrogencarbonate solution and a saturated saline solution and then dried over anhydrous magnesium sulfate
  7. customThereafter, the solvent is removed from the thus dried layer by distillation under reduced pressure
  8. customThe residue obtained
  9. customis purified by a moderate pressure column chromatography [eluent:hexane:ethyl acetate=20:1]

출처 및 근거

ORD 기록
ord-e56dfd084e2c48d28e927999c80e19bf
출처 데이터셋
uspto-grants-1999_07
특허 번호
US05922721

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