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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487316Generated: October 30, 2026

Trifluoroacetic acid → (3S,4S)-benzyl 3-amino-4-(fluoromethyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1487316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(3S,4S)-1-Cbz-N-boc-4-(fluoromethyl)pyrrolidin-3-amineHCID 68625923—
SolventDichloromethaneHCID 6344—
Product(3S,4S)-benzyl 3-amino-4-(fluoromethyl)pyrrolidine-1-carboxylateHCID 6835029899.2%

Reaction Steps

A solution of (3S,4S)-benzyl 3-((tert-butoxycarbonyl)amino)-4-(fluoromethyl)pyrrolidine-1-carboxylate (Pk1) (1.012 g, 2.87 mmol) in CH2Cl2 (10 mL) at 0° C. was added TFA (2.212 mL, 28.7 mmol) and the resulting mixture was allowed to warm to rt and stir for 1 hr. The reaction mixture was concentrated and redissolved in 70 mL of CH2Cl2 and was washed with 20 mL of 2M Na2CO3 solution and 20 mL of brine then dried over Na2SO4. Filtration and concentration afforded the title compound (0.718 g, 99% yield). 1H NMR (500 MHz, chloroform-d) δ 7.41-7.31 (m, 5H), 5.24-5.08 (m, 2H), 4.77-4.43 (m, 2H), 3.75-3.57 (m, 3H), 3.37 (s, 2H), 2.66-2.49 (m, 1H). MS(ES+) m/z: 253.2 (M+H); HPLC retention time: 1.023 min (analytical HPLC Method B). Chiral purity: 99.9% ee (chiral HPLC conditions: column: CHIRALPAK® AD-H (25×0.46 cm, 5 μm), 35% MeOH in CO2, 3 mL/min, 45° C., 220 nm, 100 bar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428511B2
Source datasetuspto-grants-2016_08
ORD IDord-4c559cb4ada64031a6b20c28139880a3
Source noteuspto-grants-2016_08