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Stannane, hydroxytrimethyl- → HCID 86702706, 화합물

HRID 1751357
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HRID 1751357 반응식
C[O:2][C:3](=[O:16])[C@@H:4]([NH:11][C:12]([O:14][CH3:15])=[O:13])[C@H:5]([O:7][CH:8]([F:10])[F:9])[CH3:6].[OH-].C[Sn+](C)C>ClC(Cl)C.C(OCC)(=O)C>[F:9][CH:8]([F:10])[O:7][C@H:5]([CH3:6])[C@H:4]([NH:11][C:12]([O:14][CH3:15])=[O:13])[C:3]([OH:16])=[O:2]
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참가 물질

5

반응물 2

HCID 11217597Stannane, hydroxytrimethyl-HCID 59610741(2S,3R)-methyl-3-(difluoromethoxy)-2-(methoxycarbonylamino)butanoate

생성물 1

HCID 86702706HCID 86702706, 화합물

시약·촉매·용매 2

HCID 63651,1-Dichloroethane용매HCID 8857Ethyl Acetate용매

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온도
80 °C
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실험 절차

To a solution of (2S,3R)-methyl-3-(difluoromethoxy)-2-(methoxycarbonylamino)butanoate (265 mg, 1.1 mmol) in dichloroethane (10 mL) was added trimethyltin hydroxide (1 g, 5.5 mmol) and the resulting mixture was heated to 80° C. for 1 hour. The reaction was cooled to room temperature, diluted with ethyl acetate, washed twice with 5% aqueous HCl solution and brine, dried (MgSO4) and concentrated. The resulting crude material (209 mg, 84%) was used without further purification.

후처리

  1. temperatureThe reaction was cooled to room temperature
  2. washwashed twice with 5% aqueous HCl solution and brine
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated
  5. customThe resulting crude material (209 mg, 84%) was used without further purification

출처 및 근거

ORD 기록
ord-db1cb3330b1d4d89bcc51399715dfb30
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09156823B2

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