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Water → 3-(4-Chlorophenyl)-2,1-benzisoxazole-7-acetonitrile

HRID 1198997
ノート
印刷プレビュー

反応式

HRID 1198997 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][N:10]=[C:11]3[C:16]([CH2:17]Br)=[CH:15][CH:14]=[CH:13][C:12]=23)=[CH:4][CH:3]=1.[C-:19]#[N:20].[K+].O1CCOCC1.O>C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][N:10]=[C:11]3[C:16]([CH2:17][C:19]#[N:20])=[CH:15][CH:14]=[CH:13][C:12]=23)=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 9032Potassium CyanideHCID 312751,4-DioxaneHCID 156347563-(4-Chlorophenyl)-7-(bromomethyl)-2,1-benzisoxazole

生成物 1

HCID 156347583-(4-Chlorophenyl)-2,1-benzisoxazole-7-acetonitrile収率 61%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane
溶媒

実験手順

A solution of 11.5 g (0.036 mole) of crude 3-(4-chlorophenyl)-7-(bromomethyl)-2,1-benzisoxazole, 9.8 g (0.15 mole) of potassium cyanide, 150 ml of dioxane and 75 ml of water was heated at reflux under a nitrogen atmosphere for 2.5 hr. The solution was cooled and poured into 400 ml of methylene chloride. The layers were separated and the organic layer was washed with four 200 ml portions of water, dried over sodium sulfate, and concentrated to give a solid as residue. The solid was recrystallized (charcoal) twice from ethyl acetate to yield 5.8 g (61%) of crystals, m.p. 165°-169° C.

後処理

  1. temperatureat reflux under a nitrogen atmosphere for 2.5 hr
  2. temperatureThe solution was cooled
  3. customThe layers were separated
  4. washthe organic layer was washed with four 200 ml portions of water
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated
  7. customto give a solid as residue
  8. customThe solid was recrystallized (charcoal) twice from ethyl acetate

出典と根拠

ORDレコード
ord-aaa339ad2e124f8c975149d421083d32
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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