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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106424Generated: October 31, 2026

Trifluoroacetic acid → HCID 131727595, compound

https://huagongshe.com/reaction/2106424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 131727596HCID 131727596—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 131727595HCID 131727595—

Reaction Steps

2 ml trifluoroacetic acid are added to a solution of 0.19 g 1-chloro-4-(β-D-glucopyranos-1-yl)-2-[4-(1-tert-butlyoxycarbonylpiperidin-4-yloxy)-benzyl]-benzene in 4 ml dichloromethane. The solution is stirred for 1.5 h at ambient temperature and then diluted with ethyl acetate and made basic with aqueous potassium carbonate solution. The organic phase is separated off and the aqueous phase is extracted with ethyl acetate. The combined organic phases are dried over sodium sulphate and the solvent is eliminated entirely.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579449B2
Source datasetuspto-grants-2009_08
ORD IDord-e5a25e96d3654de59e89e17a7fc8ed15
Source noteuspto-grants-2009_08