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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069088Generated: October 28, 2026

Trifluoroacetic acid → HCID 21191156, compound

https://huagongshe.com/reaction/1069088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 54336416HCID 54336416—
SolventDichloromethaneHCID 6344—
ProductHCID 21191156HCID 2119115698.5%

Reaction Steps

The methyl-3′-[2-[[(tert-butoxy)carbonyl]amino]ethoxy]-[1,1′-biphenyl]-3-carboxylate (659 mg) was dissolved in methylene chloride (25 mL) and trifluoroacetic acid (2.5 mL) was added. The mixture was stirred at room temperature for 6 h, additional trifluoroacetic acid (1.0 mL) was added and the mixture was stirred overnight. The mixture was concentrated and partitioned between saturated aqueous sodium bicarbonate and ethyl acetate. The organic layer was separated, dried over sodium sulfate, filtered and concentrated to give the crude product. This residue was partitioned between 1:1 hexane: ethyl acetate and 1 N aqueous HCl. The aqueous layer was separated, washed with 1:1 hexane: ethyl acetate and made basic by addition of solid sodium bicarbonate. The mixture was extracted twice with ethyl acetate, and the combined organic extracts were dried over sodium sulfate, filtered and concentrated to afford the title compound (474 mg) as a colorless oil. Electrospray MS (positive ion): (M+H) 272.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251925B1
Source datasetuspto-grants-2001_06
ORD IDord-66f9ec29f64b4aac90bd651018e8bb33
Source noteuspto-grants-2001_06