Formaldehyde → Methyl 4-(1-diphenylmethoxycarbonyl-2-hydroxyethyl)-2,3,5,6-tetrafluorobenzoate

HRID 981260노트

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HRID 981260 반응식
[C:1]1([CH:7]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[O:8][C:9]([CH2:11][C:12]2[C:21]([F:22])=[C:20]([F:23])[C:15]([C:16]([O:18][CH3:19])=[O:17])=[C:14]([F:24])[C:13]=2[F:25])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C=O.[C:34](OCC)(=[O:36])C.O>CN(C)C=O.C[O-].[Na+]>[C:26]1([CH:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[O:8][C:9]([CH:11]([C:12]2[C:13]([F:25])=[C:14]([F:24])[C:15]([C:16]([O:18][CH3:19])=[O:17])=[C:20]([F:23])[C:21]=2[F:22])[CH2:34][OH:36])=[O:10])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1

참가 물질

7

실험 절차

In 486 ml of N,N-dimethylformamide was dissolved 8.6 g of methyl 4-diphenylmethoxycarbonylmethyl-2,3,5,6tetrafluorobenzoate. To the resulting solution were added 3.54 g of paraformaldehyde and 61 mg of sodium methylate in this order. The resulting mixture was stirred at room temperature for 2 hours. To the reaction mixture were added 300 ml of ethyl acetate and 800 ml of water in this order. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue obtained was purified by a column chromatography (eluant: toluene/ethyl acetate=10/1) to obtain 35.0 g (yield: 67.0%) of methyl 4-(1-diphenylmethoxycarbonyl-2-hydroxyethyl)-2,3,5,6-tetrafluorobenzoate.

후처리

  1. customThe organic layer was separated
  2. washwashed with water
  3. dry with materiala saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate
  4. customThe solvent was removed by distillation under reduced pressure
  5. customThe residue obtained
  6. customwas purified by a column chromatography (eluant: toluene/ethyl acetate=10/1)

출처 및 근거

ORD 기록
ord-06217ae6be1b419585d3e9f8d0d05ecf
출처 데이터셋
uspto-grants-1991_02
특허 번호
US04990508

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