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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465998Generated: November 2, 2026

Trifluoroacetic acid → HCID 67326759, compound

https://huagongshe.com/reaction/1465998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 71009683HCID 71009683—
SolventDichloromethaneHCID 6344—
ProductHCID 67326759HCID 6732675986.6%

Reaction Steps

1.55 g (4.17 mmol) of tert-butyl 3-(4′-fluorobiphenyl-4-yloxymethyl)pyrrolidine-1-carboxylate are dissolved in 40 ml of dichloromethane and then, at 0° C., 6.00 ml (80.77 mmol) of trifluoroacetic acid are subsequently added. After stirring at ambient temperature for two hours, the mixture is concentrated to dryness and then the residue is taken up in water and dichloromethane. A saturated sodium hydrogencarbonate solution is added and then the aqueous phase is extracted with dichloromethane. The combined organic phases are washed with a saturated aqueous sodium chloride solution, dried over sodium sulphate, filtered and concentrated under vacuum. 0.98 g of product is obtained in the form of an oil, used as is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000010B2
Source datasetuspto-grants-2015_04
ORD IDord-2228172db5484c3e9b149137d17c7fd5
Source noteuspto-grants-2015_04