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HRID 1288519作成日:2026年10月25日

[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

https://huagongshe.com/reaction/1288519

反応式

関与物質

役割名称HCID仕込み量
反応物[1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(4-chlorobenzyl)ammonium iodideHCID 21502450—
触媒Silver ChlorideHCID 24561—
溶媒MethanolHCID 887—
生成物[1-Methyl-3-(2,6,6-trimethyl-2-cyclohexenyl)-2(trans)-propenyl]dimethyl(4-chlorobenzyl)ammonium chlorideHCID 21502481111.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03988373
出典データセットuspto-grants-1976_10
ORD IDord-ab552f525aed427d99a40a348038bef3
出典メモuspto-grants-1976_10