Thionyl Chloride → 2-Chloromethyl-3-ethoxypyridine hydrochloride

HRID 263241

反応式

HRID 263241 の反応式
S(Cl)([Cl:3])=O.[CH2:5]([O:7][C:8]1[C:9]([CH2:14]O)=[N:10][CH:11]=[CH:12][CH:13]=1)[CH3:6]>C(Cl)(Cl)Cl>[ClH:3].[Cl:3][CH2:14][C:9]1[C:8]([O:7][CH2:5][CH3:6])=[CH:13][CH:12]=[CH:11][N:10]=1

参加物

4

反応物 2

HCID 24386Thionyl ChlorideHCID 22018715(3-Ethoxypyridin-2-yl)methanol

生成物 1

HCID 204741852-Chloromethyl-3-ethoxypyridine hydrochloride

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

Thionyl chloride (8 cc) was added over 8 minutes to a stirred solution of 3-ethoxy-2-hydroxymethylpyridine (5.6 g) in chloroform (60 cc) at room temperature. After 11/2 hrs the mixture was evaporated to dryness and the residue was recrystallised from 0.16 M ethanolic hydrogen chloride/diethyl ether (1:1) to give 2-chloromethyl-3-ethoxypyridine hydrochloride (6.5 g) m.p. 176°-179.5°. (decomp.).

後処理

  1. customAfter 11/2 hrs the mixture was evaporated to dryness
  2. customthe residue was recrystallised from 0.16 M ethanolic hydrogen chloride/diethyl ether (1:1)

出典と根拠

ORDレコード
ord-0572a0990f034a81beadd8005107c15c
出典データセット
uspto-grants-1979_05
特許番号
US04156727

関連ノート

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