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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10683Generated: October 29, 2026

Pyrrolidine → 2-Pyrrolidin-1-yl-5-thiophen-2-yl-benzaldehyde

https://huagongshe.com/reaction/10683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant2-Fluoro-5-(thiophen-2-yl)benzaldehydeHCID 16768656—
SolventEthyl AcetateHCID 8857—
Product2-Pyrrolidin-1-yl-5-thiophen-2-yl-benzaldehydeHCID 2198106632%

Reaction Steps

Ex-63A: A solution of 2-fluoro-5-thiophen-2-yl-benzaldehyde (1.42 g, 6.89 mmol) in pyrrolidine was refluxed (10 mL). After 4.5 days the reaction mixture was cooled and diluted with ethyl acetate. The solution of ethyl acetate was washed with hydrochloric acid (0.5M) sodium carbonate (2M) and saturated solution of sodium bicarbonate, dried over sodium sulfate, and concentrated. The crude product was purified by flash chromatography. Elution with ethyl acetate (20%, v/v, in hexane) afforded 2-pyrrolidin-1-yl-5-thiophen-2-yl-benzaldehyde (0.5 g, 32%). 1H NMR (CDCl3) δ 10.14 (s, 1H), 7.94 (d, J=2 Hz, 1H), 7.62 (dd, J=2.7, 9 Hz, 1H), 7.22–7.20 (m, 2H), 7.07–7.04 (m, 1H), 6.86 (d, J=9 Hz, 1H), 3.41 (m, 4H), 2.01 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094801B2
Source datasetuspto-grants-2006_08
ORD IDord-db9d400ae05d48d8a73cef95d7c4ce31
Source noteuspto-grants-2006_08