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HRID 1284928생성일: 2026년 10월 26일

Butyl isocyanate → 4-Chloro-4'-(N-butyl-carbamoyloxy)-alpha-ethyl-benzhydrol

https://huagongshe.com/reaction/1284928

반응식

참여 물질

역할이름HCID투입량
반응물Butyl isocyanateHCID 8110—
반응물TriethylamineHCID 8471—
반응물alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcoholHCID 14727318—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-4'-(N-butyl-carbamoyloxy)-alpha-ethyl-benzhydrolHCID 14727325—

반응 단계

7.9 g. of 4-chloro-4'-hydroxy-α-ethyl-benzhydrol, 3.3 g. of n-butyl-isocyanate and 0.3 ml. of triethyl amine are dissolved in 40 ml. of dry tetrahydrofurane under stirring at 25° C., and the solution is allowed to stand at this temperature for 20 hours. When the reaction is complete, tetrahydrofurane is distilled off under reduced pressure, the residue is taken up in ether, the ethereal solution is shaken with a 5% aqueous sodium hydroxide solution and washed to neutral with water. The organic phase is dried over anhydrous magnesium sulfate, filtered and ether is distilled off in vacuo. Crystallization of the residue from a mixture of n-hexane and ethyl acetate yields 9.3 g. of the named compound, which melts at 78° to 79° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04564630
출처 데이터셋uspto-grants-1986_01
ORD IDord-3e65dc41c411420ea5bcad8682a8aae3
출처 메모uspto-grants-1986_01