Thionyl Chloride → 3-(Chloromethyl)-5-fluoropyridine

HRID 2200628ノート

反応式

HRID 2200628 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH2:8]O)[CH:5]=[N:6][CH:7]=1.S(Cl)([Cl:12])=O>C(Cl)Cl>[Cl:12][CH2:8][C:4]1[CH:5]=[N:6][CH:7]=[C:2]([F:1])[CH:3]=1

参加物

4

反応物 2

HCID 24386Thionyl ChlorideHCID 1524495-Fluoro-3-pyridinemethanol

生成物 1

HCID 216984253-(Chloromethyl)-5-fluoropyridine収率 76%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of (5-fluoropyridin-3-yl)methanol (0.19 g, 1.50 mmol) in DCM (5 mL) was added thionyl chloride (0.19 ml, 2.6 mmol) at 0° C. The reaction was stirred at room temperature for 2 h. The reaction was concentrated and the residue was dried in vacuo to yield 3-(chloromethyl)-5-fluoropyridine (166 mg) which was used without characterization.

後処理

  1. concentrationThe reaction was concentrated
  2. customthe residue was dried in vacuo

出典と根拠

ORDレコード
ord-f37fbb0c226c4c0a873a7e1eb170bac8
出典データセット
uspto-grants-2016_06
特許番号
US09359359B2

反応ノート

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