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HRID 462055생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/462055

반응식

참여 물질

역할이름HCID투입량
반응물AcetateHCID 175—
반응물Acetyl chlorideHCID 6367—
반응물2,2,2-TrichloroethanimidamideHCID 35608—
반응물1-Chloro-3-phenoxy-2-propanolHCID 94300—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물N-(2-acetoxy-3-phenoxypropyl) trichloroacetamidine hydrochlorideHCID 178476389—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04065464
출처 데이터셋uspto-grants-1977_12
ORD IDord-3cc1b248ecb84b97b74215c9dbb66d04
출처 메모uspto-grants-1977_12