Ammonium Chloride → 1-Chloro-10,14-dimethylnonadeca-10,13-dien-7-yne
反応式
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]#[CH:9].C([Mg]Br)C.Br[CH2:15][C:16]([CH3:27])=[CH:17][CH2:18][CH:19]=[C:20]([CH3:26])[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].[Cl-].[NH4+]>CCOCC.O1CCCC1>[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]#[C:9][CH2:15][C:16]([CH3:27])=[CH:17][CH2:18][CH:19]=[C:20]([CH3:26])[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]参加物
実験手順
A solution of 12.0 g. of 1-chlorooct-7-yne in 20 ml. of tetrahydrofuran is added to a mixture of 27 ml. of 3N ethyl magnesium bromide in ether and 50 ml. of tetrahydrofuran. The mixture is stirred and heated under reflux for 30 min. under nitrogen, then 0.45 g. of powdered cuprous chloride is added and heating and stirring is continued for 20 min. A solution of 20.0 g. of 1-bromo-2,6-dimethyl-2,5-undecadiene in 15-ml. of tetrahydrofuran is added and the mixture is heated under reflux for 10 hrs., then allowed to stand for about 18 hrs., and poured into saturated aqueous ammonium chloride and ether. The mixture is filtered and the ether solution is separated, washed with water, dried over sodium sulfate, and evaporated to leave a residue comprising 1-chloro-10,14-dimethylnonadeca-10,13-dien-7-yne.
後処理
- temperatureheated
- temperatureunder reflux for 30 min. under nitrogen
- temperatureheating
- stirringstirring
- temperaturethe mixture is heated
- temperatureunder reflux for 10 hrs
- waitto stand for about 18 hrs
- filtrationThe mixture is filtered
- customthe ether solution is separated
- washwashed with water
- dry with materialdried over sodium sulfate
- customevaporated
出典と根拠
- ORDレコード
- ord-0cca801f0c7d4f3499e42b514095badf
- 出典データセット
- uspto-grants-1976_04
- 特許番号
- US03953499
反応ノート
読み込み中…