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5-(Bromoacetyl)-2-(phenylmethoxy)benzamide → 2-(Benzyloxy)-5-(2-oxiranyl)benzamide

HRID 1281477
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HRID 1281477 반응식
[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][C:15]([C:18](=[O:21])[CH2:19]Br)=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>O1CCCC1.C(O)C>[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][C:15]([CH:18]2[CH2:19][O:21]2)=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

5

반응물 2

HCID 30183385-(Bromoacetyl)-2-(phenylmethoxy)benzamideHCID 4311764Sodium borohydride

생성물 1

HCID 99035062-(Benzyloxy)-5-(2-oxiranyl)benzamide수율 96.2%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 8028Tetrahydrofuran용매

실험 절차

2-(Benzyloxy)-5-(2-bromoacetyl)benzamide (11.3 g, 32.30 mmol) was dissolved in anhydrous tetrahydrofuran (250 mL) and cooled in an ice bath. The solution was diluted with ethanol (250 mL). Sodium borohydride (1.2 g, 32.3 mmol) was added in three portions. Following addition the solvent was removed in vacuo and the residue partitioned between water and ethyl acetate. The organic layer was washed with water, brine, and dried over anhydrous magnesium sulfate. The solution was filtered and the solvent evaporated to dryness in vacuo to yield crude title compound (1 0.88 g, 31.06 mmol).

후처리

  1. temperaturecooled in an ice bath
  2. additionaddition the solvent
  3. customwas removed in vacuo
  4. customthe residue partitioned between water and ethyl acetate
  5. washThe organic layer was washed with water, brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationThe solution was filtered
  8. customthe solvent evaporated to dryness in vacuo

출처 및 근거

ORD 기록
ord-412c3d214f844e14a6a576ed302311c6
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06451814B1

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