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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882673Generated: October 25, 2026

Tetrahydrofuran → Ethyl 3-(acetylthio)-3-cyanopropanoate

https://huagongshe.com/reaction/882673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Thiopheneacetic acidHCID 15970—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl (2Z)-3-cyanoprop-2-enoateHCID 15577688—
ProductEthyl 3-(acetylthio)-3-cyanopropanoateHCID 5324810865%

Reaction Steps

(Z)-ethyl 3-cyanoacrylate (5.01 g, 40.00 mmol) in 80 ml of THF at −20° C. was added the solution of thiol acetic acid (5.0 ml, 70.15 mmol) and DIPEA (16.0 ml, 92.03 mmol) in 20 ml of THF in 30 min. The reaction was kept at −20° C. for 4 hr then room temperature overnight. The mixture was concentrated, diluted with CH2Cl2, washed with saturated NaHCO3, dried over MgSO4, filtered, evaporated and purified by SiO2 chromatography (1:4 EtAC/Hexane) to afford 5.22 g (65%) of the title compound. Rf=0.25 (1:4 EtAC/Hexane); 1H NMR (CDCl3), 4.44 (m, 1H), 4.11 (dd, 2H, J=7.1, 14.3 Hz), 3.38 (m, 1H), 3.15 (m, 1H), 2.17 (s, 3H), 1.19 (t, 3H, J=7.2 Hz); 13C NMR 194.12, 173.21, 119.82, 61.35, 33.52, 30.08, 14.62; MS m/z+ 225.9 (MW+Na), m/z− 201.7 (MW−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236319B2
Source datasetuspto-grants-2012_08
ORD IDord-ba6cdf2b3bb44480aa7b805b882d90d0
Source noteuspto-grants-2012_08