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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870935Generated: October 30, 2026

Potassium Carbonate → 2-((Tert-butoxycarbonyl)amino)-5,5,5-trifluoropentanoic acid

https://huagongshe.com/reaction/870935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant2-Amino-5,5,5-trifluoropentanoic acid hydrochlorideHCID 71758504—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-((Tert-butoxycarbonyl)amino)-5,5,5-trifluoropentanoic acidHCID 53401930122.4%

Reaction Steps

To a stirred solution of 2-amino-5,5,5-trifluoropentanoic acid hydrochloride (400 mg, 1.503 mmol) in THF (8 mL) and water (8 mL) was added K2CO3 (831 mg, 6.01 mmol) at rt and the solution was stirred for 10 min. To this mixture was added BOC2O (656 mg, 3.01 mmol). The reaction mixture was stirred for 8 h at rt. The reaction mixture was concentrated under reduced pressure. The aq. layer was washed with ethyl acetate (3×5 mL). The aqueous layer was acidified with saturated citric acid solution (5 mL) and then extracted with ethyl acetate (3×8 mL). The combined organic layers were washed with water (3×5 mL) followed by brine (10 mL), dried over sodium sulfate and concentrated under reduced pressure to afford 2-((tert-butoxycarbonyl)amino)-5,5,5-trifluoropentanoic acid (500 mg, 1.84 mmol) quantitatively as a colorless oil. The crude material was taken as such to the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 5.04 (s, 1H), 4.38 (s, 1H), 2.15-2.28 (m, 2H), 1.91-1.95 (m, 2H), 1.46 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969564B2
Source datasetuspto-grants-2015_03
ORD IDord-ad9e49bc87574614a4d3685edb3b619f
Source noteuspto-grants-2015_03