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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604119Generated: November 1, 2026

Acetonitrile → HCID 15867813, compound

https://huagongshe.com/reaction/1604119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPyridine, hydrofluoride (1:1)HCID 64774—
ReactantHCID 15867812HCID 15867812—
SolventPyridineHCID 1049—
ProductHCID 15867813HCID 1586781379%

Reaction Steps

To a solution of ice-cooled acetonitrile (1 mL) and pyridine (10 mL) was added a hydrogen fluoride-pyridine (0.1 mL). To this solution was added methyl (11R,12S,13E,15S,17R)-9-methoxycarbonyl-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate (67 mg, 0.097 mmol) in pyridine (0.1 mL). The ice bath was removed and the solution was agitated for 15 hours while returning it to room temperature. The reaction solution was poured into a mixture of ethyl acetate and saturated aqueous sodium hydrogencarbonate. The desired product was extracted from this mixed solution with ethyl acetate. The extract was washed with brine, then dried over anhydrous sodium sulfate. The solution was concentrated under reduced pressure, then was purified by silica gel column chromatography (40 to 50% ethyl acetate/hexane) to obtain methyl (11R,12S,13E,15S,17R)-9-methoxycarbonyl-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoate (35 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990346
Source datasetuspto-grants-1999_11
ORD IDord-ebef91e7aa3a4e0fa434481fb14d3215
Source noteuspto-grants-1999_11