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HRID 1284928作成日:2026年10月26日

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

https://huagongshe.com/reaction/1284928

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl isocyanateHCID 8110—
反応物TriethylamineHCID 8471—
反応物alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcoholHCID 14727318—
溶媒TetrahydrofuranHCID 8028—
生成物4-Chloro-4'-(N-butyl-carbamoyloxy)-alpha-ethyl-benzhydrolHCID 14727325—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04564630
出典データセットuspto-grants-1986_01
ORD IDord-3e65dc41c411420ea5bcad8682a8aae3
出典メモuspto-grants-1986_01