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Chlorotrimethylsilane → (2R,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid methyl ester Hydrochloride

HRID 480074
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인쇄 미리보기

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HRID 480074 반응식
[NH2:1][C@H:2]([CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C@@H:3]([OH:7])[C:4]([OH:6])=[O:5].[Cl:15][Si](C)(C)[CH3:17]>CO>[ClH:15].[CH3:17][O:5][C:4](=[O:6])[C@H:3]([OH:7])[C@H:2]([NH2:1])[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6397ChlorotrimethylsilaneHCID 638739(2R,3R)-3-amino-2-hydroxy-4-phenylbutanoic acid

생성물 1

HCID 69746370(2R,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid methyl ester Hydrochloride

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of (2R,3R)-3-amino-2-hydroxy-4-phenylbutyric acid (200 mg, 1.0 mmol, Sigma Chemical Co. (St. Louis, Mo.), chlorotrimethylsilane (500 mg, 4.6 mmol) and methanol (2 mL) was heated at reflux for 5.5 hours and concentrated to a foam: Yield 244 mg, 100%.

후처리

  1. temperatureat reflux for 5.5 hours
  2. concentrationconcentrated to a foam

출처 및 근거

ORD 기록
ord-68e6644c97174533a932adf574bfc742
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06649634B2

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