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Sodium Hydroxide → 3-((R)-1-phenylethylamino)-2-(4-bromophenyl)propan-1-ol

HRID 515461
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반응식

HRID 515461 반응식
C([O:4][CH2:5][CH:6]([C:17]1[CH:22]=[CH:21][C:20]([Br:23])=[CH:19][CH:18]=1)[CH2:7][NH:8][C@@H:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH3:10])(=O)C.[OH-].[Na+]>CO>[C:11]1([C@H:9]([NH:8][CH2:7][CH:6]([C:17]2[CH:18]=[CH:19][C:20]([Br:23])=[CH:21][CH:22]=2)[CH2:5][OH:4])[CH3:10])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 672824433-((R)-1-phenylethylamino)-2-(4-bromophenyl)propyl acetate

생성물 1

HCID 672813523-((R)-1-phenylethylamino)-2-(4-bromophenyl)propan-1-ol수율 95%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of diastereopure 3-((R)-1-phenylethylamino)-2-(4-bromophenyl)propyl acetate (2.85 g, 7.57 mmol) in methanol (30.3 ml) was added 1.0N-sodium hydroxide (30.3 ml, 30.3 mmol) at 0° C. The mixture was stirred at room temperature for 3 hours. The mixture was partitioned between saturated ammonium chloride solution and chloroform, and the organic layer was dried over sodium sulfate. The solvent was evaporated under reduced pressure to afford diastereopure 3-((R)-1-phenylethylamino)-2-(4-bromophenyl)propan-1-ol as white solid (2.40 g, 95%).

후처리

  1. customThe mixture was partitioned between saturated ammonium chloride solution and chloroform
  2. dry with materialthe organic layer was dried over sodium sulfate
  3. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-a0d41684a1054f0a8f16bf19db0fab08
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09108957B2

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