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Methanol → 4-Chloro-DL-phenylalanine methyl ester hydrochloride

HRID 61392
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HRID 61392 반응식
[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([CH2:6][C@@H:7]([C:9]([OH:11])=[O:10])[NH2:8])=[CH:4][CH:3]=1.S(Cl)(Cl)=O.[CH3:18]O>>[ClH:1].[NH2:8][CH:7]([CH2:6][C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:13][CH:12]=1)[C:9]([O:11][CH3:18])=[O:10]
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참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 7361904-Chloro-L-phenylalanine

생성물 1

HCID 27332774-Chloro-DL-phenylalanine methyl ester hydrochloride수율 99%

실험 절차

While under nitrogen, a stirred suspension of 4-chlorophenylalanine (2.50 g, 12.5 mmol) in anhydrous methanol (18 mL) was cooled in an ice-water bath and carefully treated with thionyl chloride (1.00 mL, 13.8 mmol). After stirring for 10 min, and the cooling bath was removed and the mixture was allowed to warm to room temperature. A reflux condenser was attached, and the slurry was warmed to 55° C. After stirring overnight, the mixture was cooled to room temperature, concentrated and dried under reduced pressure to give methyl 2-amino-3-(4-chlorophenyl)propanoate hydrochloride (3.13 g, 99%) as a white solid. ESI+MS found for C10H12ClNO2 m/z 214.0 (M+H).

후처리

  1. temperaturewas cooled in an ice-water bath
  2. customthe cooling bath was removed
  3. customA reflux condenser was attached
  4. temperaturethe slurry was warmed to 55° C
  5. stirringAfter stirring overnight
  6. temperaturethe mixture was cooled to room temperature
  7. concentrationconcentrated
  8. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-fc03cc5d3a4c4b408653052474467231
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09440995B2

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