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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914447Generated: October 26, 2026

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

https://huagongshe.com/reaction/1914447

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 numberUS08613930B2
Source datasetuspto-grants-2013_12
ORD IDord-7887a71f259a4f0bbc678a3c1c5ad510
Source noteuspto-grants-2013_12