HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260476Generated: October 25, 2026
Thiophenol → 1-(Phenylthio)pyrrolidine-2,5-dione
https://huagongshe.com/reaction/260476
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Phenylthio)pyrrolidine-2,5-dione | HCID 361774 | — |
Reaction Steps
To a partial solution of N-chlorosuccinimide (3.34 g, 25 mmol) in dry methylene chloride (30 mL), cooled in an ice bath and under an inert atmosphere, was added thiophenol (2.05 mL, 20 mmol) via syringe. After stirring for 1 hour, additional N-chlorosuccinimide (0.40 g, 3 mmol) was added. After 2.5 hours total, triethylamine (3.9 mL, 28 mmol) was added dropwise. Within 15 minutes the reaction mixture was diluted with methylene chloride, the solvent washed with dilute aq. HCl and the solvent then dried (Na2SO4), filtered through a pad of charcoal and evaporated. The residue was triturated with diethyl ether and the product collected by filtration to yield the title compound mp 115°-116° C. [lit. mp 115°-116° C., J. Org. Chem., 34, 51 (1969)]. This material was used as is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05527819 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-1cdca9b0108b469eb8fecd095c52da43 |
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| Source note | uspto-grants-1996_06 |
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