Thionyl Chloride → 3-Chloromethyl-4-trifluoromethylpyridine hydrochloride
反応式
O[CH2:2][C:3]1[CH:4]=[N:5][CH:6]=[CH:7][C:8]=1[C:9]([F:12])([F:11])[F:10].O=S(Cl)[Cl:15]>C(Cl)Cl>[ClH:15].[Cl:15][CH2:2][C:3]1[CH:4]=[N:5][CH:6]=[CH:7][C:8]=1[C:9]([F:12])([F:11])[F:10]参加物
4
実験手順
To a stirred solution of 3-hydroxymethyl-4-trifluoromethylpyridine (1.11 g, 6.27 mmol) from step 1 above in CH2Cl2 (20 mL) at 0° C. was added SOCl2 (0.89 g, 7.5 nmuol) in CH2Cl2 (10 mL). The mixture was allowed to warm to room temperature and stirred for 1 h, and the solvent and excess SOCl2 were evaporated under reduced pressure. The residue was concentrated from cyclohexane (3-) to give 3-chloromethyl-4-trifluoromethylpyridine hydrochloride as a solid which was used in the next step without purification (TLC: Rf = 0.75 (1:1 hexane:EtOAc)).
後処理
- customthe solvent and excess SOCl2 were evaporated under reduced pressure
- concentrationThe residue was concentrated from cyclohexane (3-)
出典と根拠
- ORDレコード
- ord-3b1727e7aa734dc2aa105832989948a8
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05756497
反応ノート
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