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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096923Generated: October 31, 2026

Trifluoroacetic acid → HCID 23648596, compound

https://huagongshe.com/reaction/2096923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 57539233HCID 57539233—
SolventDichloromethaneHCID 6344—
ProductHCID 23648596HCID 2364859665.7%

Reaction Steps

Tert-Butyl {(1R)-1-[(difluoromethoxy)methyl]-2-[(4-fluorobenzyl)amino]-2-oxoethyl}carbamate (400 mg, 1.1 mmol) was stirred with trifluoroacetic acid (1.5 mL) and dichloromethane (2.5 mL) in an ice bath for an hour. The reaction mixture was concentrated, mixed with acetic anhydride-pyridine (1:1, 6 mL) at room temperature for 30 minutes and then diluted with ethyl acetate, washed with saturated sodium bicarbonate, brine, 0.5N HCl and brine again. The organic layer was dried, concentrated, and triturated with diethyl ether to give (2R)-2-(acetylamino)-3-(difluoromethoxy)-N-(4-fluorobenzyl)propanamide (220 mg, 65.7%) as a white solid. Mp: 162.7° C. 1H NMR (300 MHz, CDCl3): (ppm) 7.24 (dd, 2H), 7.03 (t, 2H), 6.78 (w, 1H), 6.35 (d, 1H), 6.24 (wt, 1H), 4.71 (m, 1H), 4.44 (d, 2H), 4.24 (dd, 1H), 4.01 (dd, 1H) and 2.05 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450336B2
Source datasetuspto-grants-2013_05
ORD IDord-c8d71c5205b742ff9ce851d4de9c08f4
Source noteuspto-grants-2013_05