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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350338Generated: October 30, 2026

Trifluoroacetic acid → 2-(2-(4-Ethoxycarbonylphenyl)ethynyl)pyrrolidine

https://huagongshe.com/reaction/350338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-(Tert-butoxycarbonyl)-2-[2-(4-ethoxycarbonylphenyl)ethynyl]pyrrolidineHCID 23511918—
SolventDichloromethaneHCID 6344—
Product2-(2-(4-Ethoxycarbonylphenyl)ethynyl)pyrrolidineHCID 23511914100.2%

Reaction Steps

To a stirred solution of 1-(tert-butoxycarbonyl)-2-[2-(4-ethoxycarbonylphenyl) ethynyl]pyrrolidine (2.75 g, 8 mmol) in CH2Cl2 (5 mL) was added TFA (5 mL), and the resulting mixture was stirred overnight. The mixture was concentrated in vacuo and made basic with sat. NaHCO3 and extracted with CHCl3. The extract was washed with brine, dried over MgSO4, evaporated to give 1.95 g (q.y.) 2-[2-(4-ethoxycarbonylphenyl) ethynyl]pyrrolidine as a light yellow oil. 1H-NMR (CDCl3) δ 1.38 (3 H, t, J=6.8 Hz), 1.82–2.16 (4 H, m), 3.01–3.48 (2 H, m), 4.00–4.11 (1 H, m), 4.37 (2H, q, J=6.8 Hz), 4.54–4.77 (1 H, m), 7.44–7.46 (2 H, m), 7.95–7.97 (2 H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-f09cc03ed7234bfb803cc3686150531c
Source noteuspto-grants-2007_02