戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 652598作成日:2026年10月26日

Dichloromethane → Propyl N-[[[4-[2-chloro-4-(trifluoromethyl)phenoxy]phenyl]amino]thio]-N-methylcarbamate

https://huagongshe.com/reaction/652598

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物TriethylamineHCID 8471—
反応物4-[2-Chloro-4-(trifluoromethyl)phenoxy]anilineHCID 10469327—
反応物N-chlorosulphenyl-N-methylcarbamateHCID 131714972—
生成物Propyl N-[[[4-[2-chloro-4-(trifluoromethyl)phenoxy]phenyl]amino]thio]-N-methylcarbamateHCID 20197936—

反応手順

A solution of 3.7 g of N-chlorosulphenyl-N-methylcarbamate in 10 ml of dry methylene chloride was added over 20 minutes to a stirred solution of 6.3 g of 4-[2-chloro-4-(trifluoromethyl)phenoxy]aniline in 25 ml of the same solvent containing 2.5 g of triethylamine. The reaction mixture temperature was kept at 0°-5° C. by means of an ice bath until the addition was completed, and was then allowed to rise to ambient temperature over 2.0 hours. The solvent was removed under reduced pressure and the residue was suspended in 200 ml of diethyl ether and washed three times with water. The resulting ether solution was dried (MgSO4) and the solvent was evaporated. The residue was purified by rapid chromatography on silica gel using methylene chloride as eluent. Crystallisation from diethyl ether/light petroleum gave 1, as pale buff-coloured crystals (m.p.: 61°-64° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04672139
出典データセットuspto-grants-1987_06
ORD IDord-89d7d070d5224b1ea396757c6d719c8f
出典メモuspto-grants-1987_06