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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246495Generated: November 1, 2026

Trifluoroacetic acid → HCID 131727595, compound

https://huagongshe.com/reaction/2246495

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-butyloxycarbonylpiperidin-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. The resulting solution is treated with aqueous potassium carbonate solution and the organic phase is separated. The remaining basic aqueous phase is extracted with ethyl acetate and the combined organic phases are dried over sodium sulfate. The solvent is removed under reduced pressure to yield the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687469B2
Source datasetuspto-grants-2010_03
ORD IDord-b1150d1b98ce42fdb3e4b38be2fb64ff
Source noteuspto-grants-2010_03