Dimethylformamide → 3-Chloromethyl-5-(4-trifluoromethyl-phenyl)-pyridine

HRID 33522ノート

反応式

HRID 33522 の反応式
S(Cl)([Cl:3])=O.CN(C)C=O.[F:10][C:11]([F:27])([F:26])[C:12]1[CH:17]=[CH:16][C:15]([C:18]2[CH:19]=[C:20]([CH2:24]O)[CH:21]=[N:22][CH:23]=2)=[CH:14][CH:13]=1>ClCCl>[Cl:3][CH2:24][C:20]1[CH:21]=[N:22][CH:23]=[C:18]([C:15]2[CH:16]=[CH:17][C:12]([C:11]([F:27])([F:26])[F:10])=[CH:13][CH:14]=2)[CH:19]=1

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 1519486(5-(4-(Trifluoromethyl)phenyl)pyridin-3-yl)methanol

生成物 1

HCID 691060983-Chloromethyl-5-(4-trifluoromethyl-phenyl)-pyridine

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

177 mg (0.11 ml, 1.49 mmol) thionyl chloride were added drop by drop at 0° C. to a solution of 0.1 ml N,N-dimethylformamide (DMF) and 196 mg (0.74 mmol) [5-(4-Trifluoromethyl-phenyl)-pyridin-3-yl]-methanol in 6 ml dichloromethane and stirred for 1.5 h at 0° C. The mixture was poured on ice/sodium bicarbonate solution and the organic phase separated. The water phase is extracted with dichloromethane. The combined organic phases were washed with water, dried (sodium sulphate), evaporated and the obtained material (174 mg, 81%) used without further purification.

後処理

  1. additionThe mixture was poured on ice/sodium bicarbonate solution
  2. customthe organic phase separated
  3. extractionThe water phase is extracted with dichloromethane
  4. washThe combined organic phases were washed with water
  5. dry with materialdried (sodium sulphate)
  6. customevaporated
  7. customthe obtained material (174 mg, 81%) used without further purification

出典と根拠

ORDレコード
ord-b04acf9a30034fa1a1080466a7e92ccd
出典データセット
uspto-grants-2008_09
特許番号
US07429605B2

反応ノート

読み込み中…