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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | 2-Amino-5,5,5-trifluoropentanoic acid hydrochloride | HCID 71758504 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-((Tert-butoxycarbonyl)amino)-5,5,5-trifluoropentanoic acid | HCID 53401930 | 122.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969564B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-ad9e49bc87574614a4d3685edb3b619f |
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| Source note | uspto-grants-2015_03 |
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