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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580667Generated: October 30, 2026

Water → (2-butyl-6,7-dichloro-2-cyclopentyl-2,3-dihydro-1-oxo-1H-inden-5-yl)trifluoromethanesulfonate

https://huagongshe.com/reaction/580667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
Reactant2-Butyl-6,7-dichloro-2-cyclopentyl-5-hydroxy-1-indanoneHCID 12761136—
SolventDimethylformamideHCID 6228—
Product(2-butyl-6,7-dichloro-2-cyclopentyl-2,3-dihydro-1-oxo-1H-inden-5-yl)trifluoromethanesulfonateHCID 14232970—

Reaction Steps

Racemic 2-butyl-6,7-dichloro-2-cyclopentyl-2,3-dihydro-5-hydroxy-1H-inden-1-one (34.1 g, 0.1M) was stirred in dimethylformamide (100 ml) with K2CO3 (41.5 g, 0.3M) at 25° for 20 minutes. The mixture was cooled to 15°, and trifluoromethanesulfonyl chloride (19.4 g, 0.115M) was added at 15°-20° over 20 minutes. The mixture was then stirred at 25° for 30 minutes and poured into a liter of ice and water. The oil was extracted with diethyl ether (4×125 ml) and the combined organic extracts were thoroughly washed with water, dried over (MgSO4) and concentrated under vacuum to obtain the product as a viscous amber oil weighing 47.3 g. This product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04754061
Source datasetuspto-grants-1988_06
ORD IDord-674df01524d443f7b1c95ae2281adf2f
Source noteuspto-grants-1988_06