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Methyl iodide → Benzyl [(1R)-2-methoxy-1-methylethyl]carbamate

HRID 1948387
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인쇄 미리보기

반응식

HRID 1948387 반응식
[OH:1][CH2:2][C@H:3]([NH:5][C:6](=[O:15])[O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:4].[CH3:16]I>C(#N)C.[Ag]=O>[CH3:16][O:1][CH2:2][C@H:3]([NH:5][C:6](=[O:15])[O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6328Methyl iodideHCID 6951254Benzyl ((2R)-1-hydroxypropan-2-yl)carbamate

생성물 1

HCID 86643350Benzyl [(1R)-2-methoxy-1-methylethyl]carbamate수율 71.5%

시약·촉매·용매 2

HCID 92152Silver(II) oxide촉매HCID 6342Acetonitrile용매

실험 절차

To a solution of benzyl [(1R)-2-hydroxy-1-methylethyl]carbamate (0.5 g, 2.38 mmol) in acetonitrile (20 mL), silver oxide (3.8 g, 13.09 mmol) is added followed by the addition of methyl iodide (1.94 mL, 23.8 mmol). The resultant mixture was stirred overnight at room temperature. The insoluble salt was filtered off and the filtrate was concentrated. The residue was flashed using silica and Ethyl acetate/hexanes system as eluent to give the desired product as clear oil (0.38 g).

후처리

  1. filtrationThe insoluble salt was filtered off
  2. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-623a13dc66014028b2ce2f1c8414dec1
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399489B2

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