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HRID 46780作成日:2026年10月23日

Water → 2-(4-Phenoxyphenoxy)cyclopentan-1-ol

https://huagongshe.com/ja/reaction/46780

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium borohydrideHCID 4311764—
反応物3-(4-Phenoxyphenoxy)-cyclopenten-1-eneHCID 20385751—
触媒Mercuric acetateHCID 15337—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium HydroxideHCID 14798—
生成物2-(4-Phenoxyphenoxy)cyclopentan-1-olHCID 22247676—

反応手順

A solution of 12.6 g of 3-(4-phenoxyphenoxy)-cyclopenten-1-ene in 25 ml of tetrahydrofurane is added dropwise in the course of 1 hour to a mixture of 15.9 g of mercury(II) acetate, 35 ml of water and 50 ml of tetrahydrofurane. The mixture is stirred for about 15 hours at room temperature, then 50 ml of 3 N sodium hydroxide solution are added dropwise in the course of 11/2 hours, followed by the dropwise addition in the course of 1 hour of 50 ml of a 0.5 N solution of sodium borohydride in 3 N sodium hydroxide solution. The reaction mixture is stirred for 2 hours at room temperature and precipitated mercury is removed by filtration. The filtrate is poured into ice-water and, after extraction with ether, the organic phase is washed with saturated sodium chloride solution, dried over sodium sulphate and concentrated by rotary evaporation. Fractional distillation of the residue yields 2-(4-phenoxyphenoxy)cyclopentan-1-ol as a colourless oil with a boiling point of 181°-185° C./0.001 torr.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04175137
出典データセットuspto-grants-1979_11
ORD IDord-68dcc8e1681f4418be9cbbb7c7b244ab
出典メモuspto-grants-1979_11