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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1646161생성일: 2026년 10월 26일

p-Toluenesulfonic acid → 4-Methyl-3-pentylfuran-2(5H)-one

https://huagongshe.com/reaction/1646161

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-Acetoxy-4-methyl-3-pentyl-tetrahydrofuran-2-oneHCID 19801577—
용매Acetic AcidHCID 176—
생성물4-Methyl-3-pentylfuran-2(5H)-oneHCID 1595343277.3%

반응 단계

4-Acetoxy-4-methyl-3-pentyl-tetrahydrofuran-2-one (125.33 g, 549 mmol) is placed with 2.61 g (13.7 mmol) of p-toluenesulphonic acid and held at 150° C. for 4 hours while stirring. The acetic acid which is cleaved off is distilled off over a Vigreux column. The reaction solution, cooled to room temperature, is diluted with 500 ml of ether and washed in a separating funnel with 2×200 ml of sat. NaCl solution. Drying of the ether phase over MgSO4 and concentration on a rotary evaporator as well as distillation at 100°-103° C./0.12 mbar yields 71.34 g (77.3%) of 4-methyl-3-pentyl-2(5H)furanone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05179077
출처 데이터셋uspto-grants-1993_01
ORD IDord-2aa26145304d413eb1d2861ccb503d06
출처 메모uspto-grants-1993_01