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Hydrochloric Acid → Ethyl 3-amino-2-(3,4-dimethoxyphenyl)propanoate hydrochloride

HRID 1833245
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HRID 1833245 반응식
[CH2:1]([O:3][C:4](=[O:18])[CH:5]([C:16]#[N:17])[C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:14][CH3:15])[CH:7]=1)[CH3:2].[ClH:19]>C(O)C.[Pd]>[ClH:19].[CH2:1]([O:3][C:4](=[O:18])[CH:5]([C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:14][CH3:15])[CH:7]=1)[CH2:16][NH2:17])[CH3:2]
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 12814070Ethyl cyano(3,4-dimethoxyphenyl)acetate

생성물 1

HCID 69551005Ethyl 3-amino-2-(3,4-dimethoxyphenyl)propanoate hydrochloride수율 82%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a stirred solution of cyano-(3,4-dimethoxy-phenyl)-acetic acid ethyl ester (18.1 g, 72.6 mmol) in ethanol (100 mL) was added 10% palladium on activated carbon (3.6 g) and concentrated hydrogen chloride solution (6.6 mL). The reaction mixture was hydrogenated at 50 psi for 15 hrs. The mixture was filtered through a Celite® pad and the pad was washed with ethanol (500 mL). The filtrate was collected and concentrated in vacuo to afford 3-amino-2-(3,4-dimethoxy-phenyl)-propionic acid ethyl ester hydrochloride (15 g, 82% yield) as a white solid.

후처리

  1. filtrationThe mixture was filtered through a Celite® pad
  2. washthe pad was washed with ethanol (500 mL)
  3. customThe filtrate was collected
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-4fd029fe21014410ba54ce2d344d4a8a
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067529B2

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