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HRID 706896作成日:2026年10月26日

Hexamethylphosphoramide → Ethyl 2-hydroxy-6,6-dimethylcyclohex-1-enecarboxylate

https://huagongshe.com/reaction/706896

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethylphosphoramideHCID 12679—
反応物3-Methyl-2-cyclohexen-1-oneHCID 14511—
反応物Ethyl cyanoformateHCID 69336—
反応物HCID 178418348HCID 178418348—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl 2-hydroxy-6,6-dimethylcyclohex-1-enecarboxylateHCID 67126375—

反応条件

温度-5 °C

反応手順

Into a 500 mL flame dried round-bottomed flask was added copper(I) iodide (18 g) in ether (200 mL) to give a suspension. After cooling to −5° C., methyllithium (120 mL, 1.6M in ether) was added dropwise. After stirring at −5° C. for 1 hour, 3-methylcyclohex-2-enone (5.15 mL) in 15 ml ether was added dropwise, and the mixture was stirred at −5° C. for 1 hour. After cooling to −78° C., hexamethylphosphoramide (60 mL) was added dropwise. Ethyl carbonocyanidate (23.74 mL) was added. After stirring at −78° C. for 20 minutes, the mixture was warmed up to room temperature, and stirred for 1 hour. The mixture was poured into cold water, and the layers were separated. The aqueous layer was extracted with ether (3×20 mL). The combined organic layers were washed with saturated aqueous NH4Cl (3×20 mL), dried over Na2SO4, filtered, and dried under vacuum. The crude product was added to a silica gel column and purified by eluting with 0-10% ethyl acetate in hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09174982B2
出典データセットuspto-grants-2015_11
ORD IDord-fd71c6139f574343984e3b35000a0dab
出典メモuspto-grants-2015_11