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2-Amino-3-benzoyl-alpha-(methylthio)benzeneacetonitrile → 2-Amino-3-benzoylbenzeneacetonitrile

HRID 1199012
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인쇄 미리보기

반응식

HRID 1199012 반응식
[NH2:1][C:2]1[C:7]([C:8](=[O:15])[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:6][CH:5]=[CH:4][C:3]=1[CH:16](SC)[C:17]#[N:18]>O1CCCC1.[Ni]>[NH2:1][C:2]1[C:7]([C:8](=[O:15])[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:16][C:17]#[N:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 156347292-Amino-3-benzoyl-alpha-(methylthio)benzeneacetonitrile

생성물 1

HCID 156347312-Amino-3-benzoylbenzeneacetonitrile수율 72%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 19.4 g (0.069 mole) of 2-amino-3-benzoyl-α-(methylthio)benzeneacetonitrile in 200 ml of tetrahydrofuran was added 160 g of commercial Raney nickel which had been washed three times with water and three times with tetrahydrofuran. The mixture was stirred at ambient temperature for 10 minutes and then filtered. The filtrate obtained was concentrated to give a solid residue. This residue was recrystallized from 2-propanol to yield 11.7 g (72%) of the titled compound as bronze needles, m.p. 137.5°-139° C.

후처리

  1. washhad been washed three times with water and three times with tetrahydrofuran
  2. filtrationfiltered
  3. customThe filtrate obtained
  4. concentrationwas concentrated
  5. customto give a solid residue
  6. customThis residue was recrystallized from 2-propanol

출처 및 근거

ORD 기록
ord-7b7d46b850104894a9c2fa144d565eb4
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04898874

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