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

HRID 1199012
ノート
印刷プレビュー

反応式

HRID 1199012 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

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

生成物 1

HCID 156347312-Amino-3-benzoylbenzeneacetonitrile収率 72%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 8028Tetrahydrofuran溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-7b7d46b850104894a9c2fa144d565eb4
出典データセット
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04898874

反応ノート

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