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Methyl 2-(2-cyanophenoxy)acetate → 4,5-dihydro-1,4-benzoxazepin-3(2H)-one

HRID 540347
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HRID 540347 반응식
[C:1]([C:3]1[CH:14]=[CH:13][CH:12]=[CH:11][C:4]=1[O:5][CH2:6][C:7](OC)=[O:8])#[N:2]>CO.[Ni]>[O:5]1[C:4]2[CH:11]=[CH:12][CH:13]=[CH:14][C:3]=2[CH2:1][NH:2][C:7](=[O:8])[CH2:6]1
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참가 물질

4

반응물 1

HCID 1472933Methyl 2-(2-cyanophenoxy)acetate

생성물 1

HCID 9198014,5-dihydro-1,4-benzoxazepin-3(2H)-one수율 67.4%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매2회

실험 절차

The methanol solution of methyl (2-cyanophenoxy)acetate (40 g, 0.209 mol) was added to the mixture of Raney Ni (80 g) in 500 mL of methanol. The reaction mixture was stirred at room temperature overnight under hydrogen atmosphere. Raney Ni was removed by filtration, and the filtrated was concentrated under reduced pressure to give a residue which was purified by column chromatography on silica gel (methanol/dichloromethane, 1:50) to give 23 g of product. MS obsd. (ESI+) [(M+H)+] 164.

후처리

  1. customRaney Ni was removed by filtration
  2. concentrationthe filtrated was concentrated under reduced pressure
  3. customto give a residue which
  4. customwas purified by column chromatography on silica gel (methanol/dichloromethane, 1:50)

출처 및 근거

ORD 기록
ord-50ee3a4e7691456db08c075c646dc4e7
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871756B2

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