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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35491Generated: October 29, 2026

2-Dimethylaminopyridine → HCID 56613713, compound

https://huagongshe.com/reaction/35491

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(1-Hydroxy-6-methoxycarbonylhexyl)-4-(3-t-butyldimethylsilyloxy-1-octenyl)-2-cyclopentenoneHCID 57178898—
SolventDichloromethaneHCID 6344—
ProductHCID 56613713HCID 5661371325%

Reaction Conditions

Temperature40 °C

Reaction Steps

480 mg (1.0 mmole) of 4-(3-t-butyldimethylsiloxy-1-octenyl)-5-(1-hydroxy-6-methoxycarbonylhexyl)-2-cyclopentenone was dissolved in 5 ml of dichloromethane, followed by addition of 730 mg (6 mmoles) of dimethylaminopyridine and 230 microliters (3.0 mmoles) of methanesulfonyl chloride in this order. The mixture was stirred at 40° C. for 2 hours. An aqueous solution of sodium bicarbonate was added, and the mixture was stirred with dichloromethane. The organic layers were combined, washed with a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The dried product was filtered, concentrated and subjected to silica gel column chromatography (silica gel 20 g; eluent, hexane:ethyl acetate=10:1) to give 114 mg (yield 25%) of 4-(3-t-butyldimethylsilyloxy-1-octenyl)-5-(6-methoxycarbonylhexylidene)-2-cyclopentenone. The resulting compound had the following spectral data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766147
Source datasetuspto-grants-1988_08
ORD IDord-fe1403fc89004298bf00072c68230820
Source noteuspto-grants-1988_08