戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 129801作成日:2026年10月26日

Dimethyl Sulfoxide → (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienal

https://huagongshe.com/reaction/129801

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物FarnesolHCID 445070—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienalHCID 5280598100.8%

反応手順

To a CH2Cl2 solution (15 mL) of oxalyl chloride (7.81 mL, 87.7 mmol) was added dimethyl sulfoxide (12.5 mL, 175.4 mmol) dropwise over 30 min at -60° C. The resulting clear solution was stirred at this temperature for 20 min. A solution of trans, trans-farnesol (Aldrich Chemical Co.) (15 g, 67.5 mmol) in CH2Cl2 (325 mL) was added dropwise over 15 min. The reaction mixture became cloudy white during addition. The heterogeneous reaction mixture was stirred at -60° C. for 30 min, whereupon triethylamine (56.4 mL, 405 mmol) was added dropwise over 10 min. The reaction mixture became thick. The reaction mixture was allowed to warm to RT over 1 h. Ethyl ether (800 mL) was added and the organic layer was washed with H2O (500 mL), brine (500 mL) and dried over MgSO4. Evaporation gave 15 g (100%) of title compound as a crude oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05470845
出典データセットuspto-grants-1995_11
ORD IDord-afa6e30a1fca4a3ebdbc57adcbef86cc
出典メモuspto-grants-1995_11