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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 637525생성일: 2026년 10월 26일

5-Methoxyfuran-2(5H)-one → 4-(2-p-Toluenesulfonyl-prop-2-yl)-5-methoxy-tetrahydrofuran-2-one

https://huagongshe.com/reaction/637525

반응식

참여 물질

역할이름HCID투입량
반응물5-Methoxyfuran-2(5H)-oneHCID 112042—
반응물1-(Isopropylsulfonyl)-4-methylbenzeneHCID 816792—
반응물Monosodium phosphateHCID 23672064—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매CyclohexaneHCID 8078—
생성물4-(2-p-Toluenesulfonyl-prop-2-yl)-5-methoxy-tetrahydrofuran-2-oneHCID 12882413—

반응 조건

온도-70 °C

반응 단계

1.3 ml of a cyclohexane solution of 1.95M of butyllithium was slowly added with stirring at -70° C. under an inert atmosphere to a mixture of 500 mg of isopropyl-p-tolyl sulfone and 10 ml of anhydrous tetrahydrofuran and the mixture was stirred at -70° C. for 30 minutes. A solution of 287 mg of 5-methoxy-2,5-dihydrofuran-2-one in 4 ml of tetrahydrofuran was added to the mixture over 10 minutes and the mixture was held at -70° C. for one hour and was then poured into aqueous monosodium phosphate solution at 0° C. The mixture was extracted with methylene chloride and the organic phase was washed with water, dried and evaporated to dryness under reduced pressure. The residue was crystallized from isopropyl ether to obtain 490 mg of trans dl 4-(2-p-toluenesulfonyl-prop-2-yl)-5-methoxy-tetrahydrofuran-2-one in the form of white crystals melting at 129° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04556732
출처 데이터셋uspto-grants-1985_12
ORD IDord-5fdf536d5c014562936f5b020f869c59
출처 메모uspto-grants-1985_12