戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 462055作成日:2026年10月26日

Acetate → N-(2-acetoxy-3-phenoxypropyl) trichloroacetamidine hydrochloride

https://huagongshe.com/reaction/462055

反応式

関与物質

役割名称HCID仕込み量
反応物AcetateHCID 175—
反応物Acetyl chlorideHCID 6367—
反応物2,2,2-TrichloroethanimidamideHCID 35608—
反応物1-Chloro-3-phenoxy-2-propanolHCID 94300—
溶媒Acetic AcidHCID 176—
溶媒TetrahydrofuranHCID 8028—
生成物N-(2-acetoxy-3-phenoxypropyl) trichloroacetamidine hydrochlorideHCID 178476389—

反応手順

A solution of 9.3 g. (0.05 mole) of 1-chloro-2-hydroxy-3-phenoxypropane in 100 ml. of tetrahydrofuran is mixed with a solution of 8.1 g. (0.05 mole) of trichloroacetamidine, also in tetrahydrofuran. The mixture is heated at reflux for 3 hours, and concentrated to an oil, which is taken up in benzene and washed well with water. The benzene layer is dried over magnesium sulfate, filtered, and treated with excess ethanolic hydrogen chloride to provide the crude hydroxy amidine hydrochloride. This is dissolved in glacial acetic acid and converted to the acetate by treatment with 3.5 g. (0.04 mole) of acetyl chloride at room temperature for 3 days. The reaction mixture is evaporated, treated with benzene, evaporated to dryness, and the process repeated once more with benzene, twice with toluene and twice with petroleum ether. There is afforded N-(2-acetoxy-3-phenoxypropyl) trichloroacetamidine hydrochloride, m.p. 70° to 77° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04065464
出典データセットuspto-grants-1977_12
ORD IDord-3cc1b248ecb84b97b74215c9dbb66d04
出典メモuspto-grants-1977_12