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Methanol → 2-Amino-5-chloro-alpha-(2-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol

HRID 275844
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HRID 275844 반응식
CO.[NH2:3][C:4]1[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][C:5]=1[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH2:14][NH:15][C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])=[O:7].[BH4-].[Na+]>C(OC(=O)C)C>[NH2:3][C:4]1[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][C:5]=1[CH:6]([OH:7])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH2:14][NH:15][C:16]([O:18][C:19]([CH3:20])([CH3:21])[CH3:22])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 4311764Sodium borohydrideHCID 183153772-Amino-2'-tert-butoxycarbonylaminomethyl-5-chlorobenzophenone

생성물 1

HCID 539893822-Amino-5-chloro-alpha-(2-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol수율 99.4%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

To a methanol (5 ml) solution of 2-amino-2′-tert-butoxycarbonylaminomethyl-5-chlorobenzophenone (0.5 g) was added sodium borohydride (79 mg). The mixture was stirred for 3 hours at room temperature. To the reaction mixture was added acetic acid ethyl ester (100 ml), which was washed with water and, then, dried over anhydrous MgSO4. The solvent was distilled off, and the residue was purified by means of a silica gel column chromatography to give the object 2-amino-5-chloro-α-(2-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.5 g) as a colorless oily product.

후처리

  1. washwas washed with water
  2. dry with materialdried over anhydrous MgSO4
  3. distillationThe solvent was distilled off
  4. customthe residue was purified by means of a silica gel column chromatography

출처 및 근거

ORD 기록
ord-fb242133f4ca4d78ba15ec50d239e3ba
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06352982B1

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