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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9294생성일: 2026년 10월 24일

Hexamethylphosphoramide → 5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/ko/reaction/9294

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물Carbonocyanidic acid, methyl esterHCID 28660—
반응물Lithium diisopropylamideHCID 2724682—
반응물4-(2-Benzyloxyethyl)cyclohexanoneHCID 21879605—
용매TetrahydrofuranHCID 8028—
생성물5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl esterHCID 57443243—

반응 조건

온도0 °C

반응 단계

A solution of LDA (33 ml, 1.5 M in Et2O) in THF (50 mL) at −78° C. was treated with 4-(2-benzyloxy-ethyl)-cyclohexanone (9.5 g, 40.2 mmol). The mixture was warmed to 0° C. over 30 m before re-cooling to −78° C. and adding HMPA (7 mL). Methyl cyanoformate (4.1 mL, 85 mmol) was added and the mixture was stirred for 15 m before aqueous quench and work-up. The product was purified by chromatography on SiO2 with 10% EtOAc:Hx. 5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester was isolated, 5.8 g (49%) and reduced with an equivalent of NaBH4 in MeOH at −10° C. to provide the alcohol (Intermediate R2). Intermediate R2 was purified by chromatography on SiO2 with 30 to 50% EtOAC:Hx. (˜90% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091232B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-36c0fb0cef9b4fd690399403bca865cf
출처 메모uspto-grants-2006_08