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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477576생성일: 2026년 10월 24일

Acetic acid, 2-phenoxy-, ethyl ester → 1-Phenylsulfonyl-2-oxo-3-phenoxypropane

https://huagongshe.com/ko/reaction/477576

반응식

참여 물질

역할이름HCID투입량
반응물Acetic acid, 2-phenoxy-, ethyl esterHCID 17365—
반응물Methyl phenyl sulfoneHCID 18369—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Phenylsulfonyl-2-oxo-3-phenoxypropaneHCID 15080405—

반응 조건

온도-20 °C

반응 단계

n-Butyllithium (8.5 ml, 1.6M in hexane) was added at -72° C. to a solution of methylphenyl sulfone (2.14 g, 13.7 mmol) in 80 ml of tetrahydrofuran. The reaction mixture was then allowed to warm slowly to -20° C. and maintained at this temperature for 25 minutes. It was then recooled to -72° C. and ethyl phenoxyacetate (1.48 g, 8.22 mmol) was added dropwise. The cooling bath was removed, the mixture was stirred at 20° C. for 14 hrs. and then poured into 100 ml of saturated NH4Cl and extracted with diethyl ether. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulfate and the solvent removed under reduced pressure. The crude residue was purified by column chromatography (silica gel, methylene chloride) giving 1-phenylsulfonyl-2-oxo-3-phenoxypropane, the compound of formula (2a), 800 mg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04888358
출처 데이터셋uspto-grants-1989_12
ORD IDord-2cd40da7323a4651b90ebe714304744b
출처 메모uspto-grants-1989_12