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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 574803생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/574803

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물3-Methyl-2-cyclohexen-1-oneHCID 14511—
반응물Ethyl cyanoformateHCID 69336—
반응물HCID 178418348HCID 178418348—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물Ethyl 2-hydroxy-6,6-dimethylcyclohex-1-enecarboxylateHCID 67126375—

반응 조건

온도-5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09034875B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-8704d1107f774147847f75e693aa6a78
출처 메모uspto-grants-2015_05