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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604118Generated: November 4, 2026

Methanol → HCID 15867812, compound

https://huagongshe.com/reaction/1604118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 15867790HCID 15867790—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventHCID 178418416HCID 178418416—
ProductHCID 15867812HCID 1586781238%

Reaction Steps

Methyl (11R,12S,13E,15S,17R)-9-trifluoromethanesulfonyloxy-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate (388 mg, 0.5 mmol), palladium acetate (11.2 mg, 0.05 mmol), and triphenylphospine (26.2 g, 0.1 mmol) were dissolved in dimethylformamide (2 mL). To this were added methanol (810 μl, 20 mmol) and triethylamine (139 μl, 1 mmol). This was agitated in carbon monoxide atmosphere (1 atmosphere) at room temperature for 18 hours. 10 ml of water was added, the solution separated, and the aqueous phase was extracted with ether and the extract combined with the organic layer. The organic solution was washed with brine, then was dried over anhydrous sodium sulfate. The solution was concentrated under reduced pressure, then was purified by silica gel column chromatography (4% ethyl acetate/hexane) to obtain methyl (11R,12S,13E,15S,17R)-9-methoxycarbonyl-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate (134 mg, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990346
Source datasetuspto-grants-1999_11
ORD IDord-a72e1cf8cafc48f38d84f84bf2c6c031
Source noteuspto-grants-1999_11