Pyridine → 4-[(Chloromethyl)sulfanyl]pyridine

HRID 1196864

반응식

HRID 1196864 반응식
[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

참가 물질

5

실험 절차

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.

후처리

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

출처 및 근거

ORD 기록
ord-abb8f79711af4e5884a112e7965ac866
출처 데이터셋
uspto-grants-1992_05
특허 번호
US05116833

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