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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470619Generated: November 1, 2026

Trifluoroacetic acid → HCID 67396190, compound

https://huagongshe.com/reaction/470619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67395639HCID 67395639—
SolventDichloromethaneHCID 6344—
ProductHCID 67396190HCID 67396190—

Reaction Conditions

Temperature25 °C

Reaction Steps

Trifluoroacetic acid (5 mL) was added slowly into a solution of 4-{5-[2-(3,4-dimethoxy-phenyl)-vinyl]-[1,2,4]oxadiazol-3-ylmethyl}-piperidine-1-carboxylic acid tert-butyl ester (compound of Example 18; 4.5 g, 10.4 mmol) in dichloromethane (25 mL) and was stirred at 25° C. for 15 h. The solvent was evaporated and the residue was extracted into chloroform (2×25 mL). The combined organic layers were washed with saturated sodium carbonate solution (2×25 mL) and water (1×25 mL). The organic phase obtained was dried over anhydrous sodium sulphate and concentrated to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629277B2
Source datasetuspto-grants-2014_01
ORD IDord-59b3371814754f8a95316be33a44fe4a
Source noteuspto-grants-2014_01