Sodium Cyanide → Methyl 1-cyanoindan-4-carboxylate

HRID 1763424

反応式

HRID 1763424 の反応式
Cl[CH:2]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11]([O:13][CH3:14])=[O:12])[C:5]=2[CH2:4][CH2:3]1.[C-:15]#[N:16].[Na+]>CS(C)=O>[C:15]([CH:2]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11]([O:13][CH3:14])=[O:12])[C:5]=2[CH2:4][CH2:3]1)#[N:16]

参加物

4

実験手順

In 80 ml. of dimethylsulfoxide is dissolved 15 g. of methyl 1-chloroindan-4-carboxylate and the solution is stirred. Then, 5.3 g. of sodium cyanide is added, followed by stirring for 8 hours. Following the addition of 750 ml. of water, the reaction mixture is extracted with ether. The extract is washed with a saturated aqueous solution of sodium chloride and, then, dried. The solvent is distilled off under reduced pressure and the residue is purified by column chromatography on silica gel (500 g. silica gel; eluant: chloroform). The described procedure gives methyl 1-cyanoindan-4-carboxylate as crystals melting at 76.5°-77.5° C.

後処理

  1. additionthe addition of 750 ml
  2. extractionof water, the reaction mixture is extracted with ether
  3. washThe extract is washed with a saturated aqueous solution of sodium chloride
  4. customdried
  5. distillationThe solvent is distilled off under reduced pressure
  6. customthe residue is purified by column chromatography on silica gel (500 g. silica gel; eluant: chloroform)

出典と根拠

ORDレコード
ord-281ea42d330a43db8ff19d08ef42a03c
出典データセット
uspto-grants-1978_09
特許番号
US04111997

関連ノート

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