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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197042Generated: November 2, 2026

Acetic Acid → 2-Methylthio-5-(1-methoxycarbonylhexyl)-4-(3-hydroxy-1-octenyl)-2-cyclopentenone

https://huagongshe.com/reaction/1197042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Methylthio-5-(1-hydroxy-6-methoxycarbonylhexyl)-4-(3-t-butyldimethylsilyloxy-1-octenyl)-2-cyclopentenoneHCID 57243052—
SolventTolueneHCID 1140—
Product2-Methylthio-5-(1-methoxycarbonylhexyl)-4-(3-hydroxy-1-octenyl)-2-cyclopentenoneHCID 5712689965%

Reaction Steps

To 350 mg of 2-methylthio-5-(1-hydroxy-6-methoxycarbonylhexyl)-4-(3-t-butyldimethylsilyloxy-1-octenyl)-2-cyclopentenone obtained in Example 6 was added a solvent mixture of 10 ml of acetic acid, 5 ml of tetrahydrofuran, and 5 ml of water, and the mixture was stirred for 24 hours. Toluene was then added, and after concentration, the concentrate was diluted with saturated aqueous sodium hydrogencarbonate and extracted with ethyl acetate. Subsequently, the extract was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated, followed by silica gel chromatography to give 178 mg (yield 65%) of 2-methylthio-5-(1-methoxycarbonylhexyl)-4-(3-hydroxy-1-octenyl)-2-cyclopentenone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116869
Source datasetuspto-grants-1992_05
ORD IDord-1171379d35ab4c269882b94c1226a591
Source noteuspto-grants-1992_05