Water → [4-(3,4-Dichloro-benzyloxy)-phenyl]-oxo-acetaldehyde

HRID 391857

반응식

HRID 391857 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:11])[CH:9]=[O:10])=[CH:4][CH:3]=1.[Cl:12][C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][C:20]=1[Cl:21])[CH2:16]Br.C(=O)([O-])[O-].[K+].[K+].O>CN(C=O)C>[Cl:12][C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][C:20]=1[Cl:21])[CH2:16][O:1][C:2]1[CH:3]=[CH:4][C:5]([C:8](=[O:11])[CH:9]=[O:10])=[CH:6][CH:7]=1

참가 물질

6

반응물 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 905684-HydroxyphenylglyoxalHCID 6397264-(Bromomethyl)-1,2-dichlorobenzene

생성물 1

HCID 86654900[4-(3,4-Dichloro-benzyloxy)-phenyl]-oxo-acetaldehyde수율 84.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of (4-hydroxy-phenyl)-oxo-acetaldehyde (756 mg) in dry DMF (10 mL) were added 3,4-dichlorobenzylbromide (1.2 g) and potassium carbonate (1.03 g). After 4 hours, the reaction mixture was poured into water (100 mL) and extracted with ethyl acetate (2×50 mL). The organic extracts were combined and washed with brine (2×50 mL) and saturated sodium bicarbonate solution (2×50 mL). The organic layer was dried over sodium sulfate and concentrated under reduced pressure to give [4-(3,4-dichloro-benzyloxy)-phenyl]-oxo-acetaldehyde (1.3 g).

후처리

  1. extractionextracted with ethyl acetate (2×50 mL)
  2. washwashed with brine (2×50 mL) and saturated sodium bicarbonate solution (2×50 mL)
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-b3e5f75972c04d9483d0963fc18e7986
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08383644B2

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