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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1721652생성일: 2026년 10월 26일

p-Toluenesulfonic acid → Methyl (4E)-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate

https://huagongshe.com/reaction/1721652

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Mycophenolic AcidHCID 446541—
용매MethanolHCID 887—
생성물Methyl (4E)-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoateHCID 64786851,243.2%

반응 단계

A solution of 15.1 g (47.1 mmol) of (E)-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid (mycophenolic acid) and 0.7 g (3.7 mmol) of p-toluenesulfonic acid in 400 ml of methanol was allowed to stand at room temperature for 3 days. The mixture was concentrated under reduced pressure to approximately 75 ml and then partitioned between aqueous sodium bicarbonate and ethyl acetate. The organic phase was further washed with brine and then dried over sodium sulfate. Concentration of the organic phase under reduced pressure gave 15.4 g (46.0 mmol, 98%) of methyl (E)-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate as a white solid, mp 104°-105° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05512568
출처 데이터셋uspto-grants-1996_04
ORD IDord-cd5a460ab0774e4c99b345f544b78588
출처 메모uspto-grants-1996_04