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Water → (RS)-1-(4-benzyloxy-phenyl)-3-bromo-pyrrolidin-2-one

HRID 1768127
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반응식

HRID 1768127 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([NH:15][C:16](=[O:22])[CH:17]([Br:21])[CH2:18][CH2:19]Br)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].O>ClCCl>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([N:15]2[CH2:19][CH2:18][CH:17]([Br:21])[C:16]2=[O:22])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 23614762(RS)-N-(4-Benzyloxy-phenyl)-2,4-dibromo-butyramide

생성물 1

HCID 23614761(RS)-1-(4-benzyloxy-phenyl)-3-bromo-pyrrolidin-2-one수율 35%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

6.1 g (14.3 mmol) (RS)—N-(4-benzyloxy-phenyl)-2,4-dibromo-butyramide and 0.1 g of Dowex 2×10 are suspended in 50 ml dichloromethane. 7 ml of a 50% aqueous sodium hydroxide solution is slowly added under vigorous stirring. The resulting reaction mixture is stirred overnight at RT, then poured into 25 ml of cold water. The organic phase is separated, dried and evaporated. The crude material is recrystallised from ethyl acetate to yield 1.72 g (35%) of a brownish solid. Mp=125–126° C.

후처리

  1. customThe resulting reaction mixture
  2. customThe organic phase is separated
  3. customdried
  4. customevaporated
  5. customThe crude material is recrystallised from ethyl acetate

출처 및 근거

ORD 기록
ord-89e12858f1074c73be43b82f1e571513
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07235581B2

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