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HRID 1284927생성일: 2026년 10월 27일

Butyl isocyanate → 1-(3-Trifluoromethylphenyl)-1-(4-butylaminocarbonyloxyphenyl)-1-propanol

https://huagongshe.com/reaction/1284927

반응식

참여 물질

역할이름HCID투입량
반응물Butyl isocyanateHCID 8110—
반응물TriethylamineHCID 8471—
반응물Potassium HydroxideHCID 14797—
반응물3-Trifluoromethyl-4'-hydroxy-alpha-ethylbenzhydrolHCID 181876—
용매BenzeneHCID 241—
생성물1-(3-Trifluoromethylphenyl)-1-(4-butylaminocarbonyloxyphenyl)-1-propanolHCID 14727324—

반응 단계

8.9 g. of 3-trifluoromethyl-4'-hydroxy-α-ethyl-benzhydrol, 3.3 g. of n-butyl-isocyanate and 0.06 ml. of triethyl amine in 45 ml. of dry benzene are heated up to 50° C. under stirring, and the reaction mixture is kept at the same temperature for one additional hour. The progress of the reaction is monitored by thin layer chromatography. When the reaction is complete, the mixture is cooled to room temperature, the benzene solution is shaken with a 5% aqueous potassium hydroxide solution and washed to neutral with water. The organic phase is dried over anhydrous magnesium sulfate, filtered, and the solvent is distilled off under reduced pressure. The solid residue is crystallized from a mixture of ethyl acetate and n-hexane. 11.4 g. of the named compound are obtained, melting at 99° to 100° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04564630
출처 데이터셋uspto-grants-1986_01
ORD IDord-f076cec6be3d4570b8a05b9fb53c40d8
출처 메모uspto-grants-1986_01