Sodium Cyanide → Benzeneacetonitrile, 2,3-dichloro-

HRID 1800823

반응식

HRID 1800823 반응식
[Cl:1][C:2]1[C:9]([Cl:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4]Cl.[C-:11]#[N:12].[Na+]>CS(C)=O.O>[Cl:1][C:2]1[C:9]([Cl:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][C:11]#[N:12]

참가 물질

5

실험 절차

2,3-Dichlorobenzylchloride (5.0 g, 25.5 mmol) was dissolved in 100 ml DMSO. 9.2 g NaCN (188 mmol) were added and the mixture stirred at room temperature for 16 hours. The reaction mixture was diluted with water, and the product extracted with ether. The organic layers were washed with water (2×) and brine, then dried over magnesium sulfate, filtered and concentrated. The product was used as. Crude yield˜quantitative. An analytical sample was purified by column chromatography on silica, using a gradient from 10% to 75% dichloromethane in hexanes as eluent. The combined aqueous layers and wash liquids were treated with 100 ml bleach to oxidize the excess cyanide to less toxic materials.

후처리

  1. extractionthe product extracted with ether
  2. washThe organic layers were washed with water (2×) and brine
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customAn analytical sample was purified by column chromatography on silica
  7. washThe combined aqueous layers and wash liquids
  8. additionwere treated with 100 ml bleach

출처 및 근거

ORD 기록
ord-95132224f2204bf5be33c7423de2b104
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08343999B2

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