Pyridine → HCID 86762710、化合物
反応式
[CH2:1](O)[CH2:2]/[CH:3]=[CH:4]\[CH2:5][CH2:6]/[CH:7]=[CH:8]\[CH:9]=[CH:10]\[CH2:11][CH3:12].N1C=CC=CC=1.CN(C)C=O.CS([Cl:29])(=O)=O>CCCCCC.O>[Cl:29][CH2:1][CH2:2]/[CH:3]=[CH:4]\[CH2:5][CH2:6]/[CH:7]=[CH:8]\[CH:9]=[CH:10]\[CH2:11][CH3:12]参加物
反応条件
- 温度
- 7.5 °C
実験手順
(Z,Z,E)-3,7,9-Dodecatrien-1-ol (169.47 g, 0.94 mol), pyridine (134.2 g, 1.70 mol) and N,N-dimethylformamide (284 g) were placed in a reaction vessel, and stirred at 5 to 10° C. for 30 minutes. After stirring, methanesulfonyl chloride (151.2 g, 1.32 mol) was added dropwise thereto at 5 to 15° C. After completion of the dropwise addition, the reaction mixture was stirred at 60 to 65° C. for 2 hours. Then, water (471 g) was added to the reaction mixture to terminate the reaction. Hexane (471 g) was added thereto to separate the reaction mixture into phases. The organic phase was washed with hydrochloric acid and then with an aqueous sodium bicarbonate solution, and then concentrated by removal of the solvent under reduced pressure. The residue was distilled under reduced pressure to obtain (Z,Z,E)-1-chloro-3,7,9-dodecatriene (bp: 114 to 120° C./5 mmHg, 166.93 g, 0.84 mol) with a yield of 89.2%.
後処理
- stirringAfter stirring
- customat 5 to 15° C
- additionAfter completion of the dropwise addition
- stirringthe reaction mixture was stirred at 60 to 65° C. for 2 hours
- customto terminate
- customthe reaction
- customto separate the reaction mixture into phases
- washThe organic phase was washed with hydrochloric acid
- concentrationwith an aqueous sodium bicarbonate solution, and then concentrated by removal of the solvent under reduced pressure
- distillationThe residue was distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-35ca9c29b0764a1cadceb029af52b8c9
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08829255B1
反応ノート
読み込み中…