[1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(4-chlorobenzyl)ammonium iodide → [1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(4-chlorobenzyl)ammonium chloride
反応式
[I-].[CH3:2][CH:3]([N+:15]([CH3:25])([CH3:24])[CH2:16][C:17]1[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][CH:18]=1)/[CH:4]=[CH:5]/[CH:6]1[C:11]([CH3:13])([CH3:12])[CH2:10][CH2:9][CH:8]=[C:7]1[CH3:14]>[Ag]Cl.CO>[Cl-:23].[CH3:2][CH:3]([N+:15]([CH3:25])([CH3:24])[CH2:16][C:17]1[CH:18]=[CH:19][C:20]([Cl:23])=[CH:21][CH:22]=1)/[CH:4]=[CH:5]/[CH:6]1[C:11]([CH3:13])([CH3:12])[CH2:10][CH2:9][CH:8]=[C:7]1[CH3:14]参加物
4
反応物 1
生成物 1
試薬・触媒・溶媒 2
実験手順
A mixture of [1-methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(4-chlorobenzyl)ammonium iodide (2.0 g), silver chloride (1.0 g) and absolute methanol (50 cc) was refluxed for 2 hours, and the reaction mixture was filtered. The solvent of the filtrate was distilled off to give hygroscopic colorless crystals (0.9 g) of [1-methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(4-chlorobenzyl)ammonium chloride.
後処理
- temperaturewas refluxed for 2 hours
- filtrationthe reaction mixture was filtered
- distillationThe solvent of the filtrate was distilled off
出典と根拠
- ORDレコード
- ord-ab552f525aed427d99a40a348038bef3
- 出典データセット
- uspto-grants-1976_10
- 特許番号
- US03988373
反応ノート
読み込み中…