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Ammonia → (2R,3S)-3-(4-methoxyphenyl)-2,3-epoxypropionamide

HRID 1457254
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HRID 1457254 반응식
C[O:2][C:3](=O)[C@@H:4]1[O:6][C@H:5]1[C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=1.[NH3:16]>CN(C)C=O>[CH3:14][O:13][C:10]1[CH:11]=[CH:12][C:7]([C@@H:5]2[O:6][C@H:4]2[C:3]([NH2:16])=[O:2])=[CH:8][CH:9]=1
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 158607Methyl (2R,3S)-3-(4-methoxyphenyl)-2-oxiranecarboxylate

생성물 1

HCID 10821599(2R,3S)-3-(4-methoxyphenyl)-2,3-epoxypropionamide수율 85%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a mixture of (2R,3S)-3-(4-methoxyphenyl)-2,3-epoxypropionic acid methyl ester (2.08 g) and N,N-dimethylformamide (3 ml) is added 28% aqueous ammonia (6.1 g) under ice-cooling. The mixture is reacted at room temperature for two hours, and the precipitated crystals are collected by filtration, washed with water, and dried at 50° C. to give (2R,3S)-3-(4-methoxyphenyl)-2,3-epoxypropionamide (1.64 g).

후처리

  1. temperaturecooling
  2. customThe mixture is reacted at room temperature for two hours
  3. filtrationthe precipitated crystals are collected by filtration
  4. washwashed with water
  5. customdried at 50° C.

출처 및 근거

ORD 기록
ord-b348ca99a0de49b6abd77e4ed58521b4
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05847122

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