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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632248Generated: October 25, 2026

Tetrahydrofuran → 3-(4-Nitrobenzoyl)-1,3-thiazolidine-2-thione

https://huagongshe.com/reaction/1632248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant2-ThiazolidinethioneHCID 2723699—
SolventTriethylamineHCID 8471—
Product3-(4-Nitrobenzoyl)-1,3-thiazolidine-2-thioneHCID 77230973.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 4-nitrobenzoyl chloride (3.1 g) and tetrahydrofuran (50 ml) were added 1,3-thiazolidine-2-thione (2.0 g) and triethyl amine (2.5 g). The mixture was stirred at 50° C. for 30 minutes under nitrogen atmosphere. The reaction mixture was filtered and the solvent was removed at a reduced pressure. To the residue was added water, and the solution is extracted with dichloromethane. The extract was washed with a saturated aqueous solution of sodium chloride and dried with use of Glauber's salt. The solvent was distilled off and the resulting crystals were purified by silica gel column chromatography (developer: dichloromethane) and recrystallized from dichloromethane to obtain 3.3 g of the desired compound as yellow needle crystals (yield 82.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474814
Source datasetuspto-grants-1984_10
ORD IDord-c4d3668f304a4101990443742a0e5fe2
Source noteuspto-grants-1984_10