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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 2-Thiazolidinethione | HCID 2723699 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-(4-Nitrobenzoyl)-1,3-thiazolidine-2-thione | HCID 772309 | 73.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04474814 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-c4d3668f304a4101990443742a0e5fe2 |
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| Source note | uspto-grants-1984_10 |
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