Pyridine → 4-[(Chloromethyl)sulfanyl]pyridine

HRID 1196864

反応式

HRID 1196864 の反応式
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1.[Cl:9]N1C(=O)CCC1=O.N1C=CC=CC=1>C1C=CC=CC=1>[Cl:9][CH2:1][S:2][C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1

参加物

5

実験手順

A solution of 4-methylthiopyridine (2.28 g, 18.2 mmol), N-chlorosuccinimide (3.0 g, 23 mmol) and pyridine (2.9 mL, 3.0 mmol) in benzene (40 mL) was heated at 50°-60° C. for 3 h. The mixture was allowed to cool to room temperature. The solvent was decanted and the residue was rinsed with benzene (2×10 mL). The organic phases were combined and evaporated. The residue was passed through a pad of silica gel (40 g) to give the title material (1.35 g) contaminated with the starting material. The impure product was repurified on silica gel preparative plates (eluted with CH2Cl2 /CH3CN: 1/1) to give the pure title material (926 mg, 32%) as a yellow oil.

後処理

  1. customThe solvent was decanted
  2. washthe residue was rinsed with benzene (2×10 mL)
  3. customevaporated

出典と根拠

ORDレコード
ord-abb8f79711af4e5884a112e7965ac866
出典データセット
uspto-grants-1992_05
特許番号
US05116833

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