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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253039Generated: October 30, 2026

Trifluoroacetic acid → HCID 11625833, compound

https://huagongshe.com/reaction/2253039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67073371HCID 67073371—
SolventDichloromethaneHCID 6344—
ProductHCID 11625833HCID 1162583395%

Reaction Steps

The solution of 0.30 g (0.6 mmol) (R)-2-{3-chloro-4-[5-(4-methoxy-phenyl)-[1,2,4]oxadiazol-3-ylmethoxy]-benzyl}-morpholine-4-carboxylic acid tert-butyl ester in 3 mL dichloromethane was cooled to 0° C. and treated with 1.5 mL (19.6 mmol) trifluoroacetic acid. The cooling bath was removed and the solution stirred at room temperature for 1 h. The volatile components were evaporated and the residue dissolved in dichloromethane and extracted with 1N aqueous sodium hydroxide solution. The organic layer was washed with brine, dried over magnesium sulfate, evaporated and dried under high vacuum to give 0.23 g (95%) of the product as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323466B2
Source datasetuspto-grants-2008_01
ORD IDord-2950aaa088174efe80648d9f3799d19c
Source noteuspto-grants-2008_01