Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424350Generated: October 25, 2026

Tetrahydrofuran → Ethyl 5-phenyl-1,3,4-thiadiazole-2-carboxylate

https://huagongshe.com/reaction/1424350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLawesson's reagentHCID 87949—
ReactantEthyl 2-(2-benzoylhydrazinyl)-2-oxoacetateHCID 13013233—
ProductEthyl 5-phenyl-1,3,4-thiadiazole-2-carboxylateHCID 6730690056%

Reaction Steps

To a solution of ethyl 2-(2-benzoylhydrazinyl)-2-oxoacetate (1 g, 4.23 mmol) in dry THF (5 ml, 61.0 mmol) was added the Lawesson's Reagent (1.079 g, 2.67 mmol). The reaction was stirred at r.t. for 2 h without any reaction. The mixture was then heated to 50° C. and then heated to reflux. Additional Lawesson's Reagent (1.079 g, 2.67 mmol) was added and after 16 h at reflux, the reaction was halfway completed. The mixture was evaporated to dryness and the residue was purified by silica gel column chromatography (50% CH2Cl2/hexanes up to 100% CH2Cl2) to provide the title material (0.35 g, 35%). LC (Method B): 2.063 min, LCMS (APCI) calcd for C11H11N2O2S [M+H]+ m/z 235.05. found 235.0. 1H NMR (CDCl3, 400 MHz) δ ppm: 1.49 (t, J=1.00 Hz, 3H), 4.55 (q, J=1.00 Hz, 2H), 7.45-7.65 (m, 3H), 8.02-8.07 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927688B2
Source datasetuspto-grants-2015_01
ORD IDord-fce95a84e9a442d382a4e98aebd65180
Source noteuspto-grants-2015_01