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Ammonia → HCID 22792277, 화합물

HRID 1283946
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HRID 1283946 반응식
Br[CH:2]([CH3:15])[C:3]([NH:5][C:6]([CH3:14])([CH3:13])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:4].[NH3:16]>C(O)C>[CH3:13][C:6]([NH:5][C:3](=[O:4])[C@H:2]([CH3:15])[NH2:16])([CH3:14])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 215169672-Bromo-N-(2-phenylpropan-2-yl)propanamide

생성물 1

HCID 22792277HCID 22792277, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 2-bromo-N-(α,α-dimethylbenzyl)propionamide (24.0 g; 0.088 mole) in ethanol (500 ml) was cooled to 0°C. The solution was saturated with ammonia (5 hours). Stirring was continued at room temperature for about 7 days. The solvent was removed under vacuum. The oily residue was taken up in benzene. The benzene phase was extracted with 5N HCl. The aqueous phase was washed with ether, made alkaline with 5N NaOH, saturated with NaCl and extracted several times with benzene. The benzene solution was dried over anhydrous Na1SO4 and the solvent was evaporated. The N1 -(α,α-dimethylbenzyl)alanineamide was obtained as an almost colourless oil. Yield: 14.6 g (79.8 %).

후처리

  1. customThe solvent was removed under vacuum
  2. extractionThe benzene phase was extracted with 5N HCl
  3. washThe aqueous phase was washed with ether
  4. extractionsaturated with NaCl and extracted several times with benzene
  5. dry with materialThe benzene solution was dried over anhydrous Na1SO4
  6. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-c2d63f9f36144c0e9779555d70fcbb70
출처 데이터셋
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03976771

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