Triethylamine → HCID 14719431、化合物

HRID 1085375

反応式

HRID 1085375 の反応式
[CH2:1]([O:19][CH2:20][CH2:21][CH2:22][OH:23])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[CH3:24][S:25](Cl)(=[O:27])=[O:26].C(N(CC)CC)C>ClCCl>[CH3:24][S:25]([O:23][CH2:22][CH2:21][CH2:20][O:19][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])(=[O:27])=[O:26]

参加物

5

実験手順

In dichloromethane (50 ml) is dissolved 3-(octadecyloxy)propanol (8.0 g). To the solution are added, under ice-cooling, methanesulfonyl chloride (4.18 g) and triethylamine (5.1 ml). The mixture is stirred at room temperature for one hour. The reaction mixture is washed with water and an aqueous solution of sodium hydrogencarbonate, successively, and then dried. The solvent is distilled off under reduced pressure to give the above-titled compound (9.7 g).

後処理

  1. additionTo the solution are added, under ice-
  2. temperaturecooling
  3. washThe reaction mixture is washed with water
  4. dry with materialan aqueous solution of sodium hydrogencarbonate, successively, and then dried
  5. distillationThe solvent is distilled off under reduced pressure

出典と根拠

ORDレコード
ord-5231a62ac23d4fbd8898c56889ce6997
出典データセット
uspto-grants-1991_04
特許番号
US05008454

関連ノート

読み込み中…