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Sodium methanethiolate → 5-Chloro-2-methylthio-3-pyridinecarbonitrile

HRID 368282
ノート
印刷プレビュー

反応式

HRID 368282 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]#[N:10])[CH:5]=[N:6][C:7]=1Cl.[CH3:11][S-:12].[Na+]>CS(C)=O>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]#[N:10])[C:5]([S:12][CH3:11])=[N:6][CH:7]=1
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 2

HCID 4378561Sodium methanethiolateHCID 128784645,6-Dichloropyridine-3-carbonitrile

生成物 1

HCID 232882615-Chloro-2-methylthio-3-pyridinecarbonitrile収率 71%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

5,6-Dichloro-3-pyridinecarbonitrile (1.73 g, 0.01 mol) was dissolved with stirring in dimethyl sulphoxide (25 mL) and sodium methanethiolate (0.77 g, 0.011 mol) added. The reaction mixture was stirred at room temperature for two hours and poured onto ice (100 g). The mixture was extracted with dichloromethane (50 mL), and the organic extract washed with water (100 mL), and brine, and dried over anhydrous sodium sulphate. Evaporation of the solvent under reduced pressure and recrystallisation of the residue from ethyl acetate:hexane gave the desired product (1.3 g, 71%) as a cream solid, MP 147-9° C.

後処理

  1. additionpoured onto ice (100 g)
  2. extractionThe mixture was extracted with dichloromethane (50 mL)
  3. extractionthe organic extract
  4. washwashed with water (100 mL), and brine
  5. dry with materialdried over anhydrous sodium sulphate
  6. customEvaporation of the solvent
  7. customunder reduced pressure and recrystallisation of the residue from ethyl acetate

出典と根拠

ORDレコード
ord-726385f03c9446b5ae77352515a07821
出典データセット
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06133294

反応ノート

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