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Triethylamine → Methyl 2-diazo-7-methoxy-3-oxoheptanoate

HRID 1509550
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인쇄 미리보기

반응식

HRID 1509550 반응식
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7](=[O:13])[CH2:8][C:9]([O:11][CH3:12])=[O:10].C(NC1C=CC(S([N:27]=[N+:28]=[N-])(=O)=O)=CC=1)(=O)C.C(N(CC)CC)C>C(#N)C>[N+:27](=[C:8]([C:7](=[O:13])[CH2:6][CH2:5][CH2:4][CH2:3][O:2][CH3:1])[C:9]([O:11][CH3:12])=[O:10])=[N-:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 51291854-Acetamidobenzenesulfonyl azideHCID 58355424Methyl 7-methoxy-3-oxoheptanoate

생성물 1

HCID 76731428Methyl 2-diazo-7-methoxy-3-oxoheptanoate수율 121.8%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution (100 ml) of methyl 7-methoxy-3-oxoheptanoate (5.00 g) and 4-(acetylamino)benzenesulfonyl azide (7.02 g) in acetonitrile was added triethylamine (11.1 ml) and the mixture was stirred at room temperature for 2 days. Insoluble material was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was suspended in diethyl ether and the insoluble material was filtered off. The filtrate was concentrated under reduced pressure to give the object product (6.93 g).

후처리

  1. filtrationInsoluble material was filtered through celite
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. filtrationthe insoluble material was filtered off
  4. concentrationThe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-87a3630dc7fa412bacfa94095e036763
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09221836B2

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