HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657029Generated: October 26, 2026
Hydrochloric Acid → S,N-dimethyl-N'-nitro-N-trichloromethanesulfenylisothiourea
https://huagongshe.com/reaction/1657029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trichloromethanesulfenyl chloride | HCID 11666 | — |
| Reactant | 1,2-Dimethyl-3-nitroisothiourea | HCID 136227017 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | S,N-dimethyl-N'-nitro-N-trichloromethanesulfenylisothiourea | HCID 73653906 | 57.1% |
Reaction Steps
To a cooled, stirred mixture of S,N-dimethyl-N'-nitroisothiourea (1.0 g), triethylamine (0.68 g) and DMF (10 ml) was added 1.2 g of trichloromethanesulfenyl chloride dropwise at 3°-7° C. After stirring at the same temperature for 1 hour, the mixture was poured into 50 ml of 2N hydrochloric acid and the resulting mixture was extracted with toluene (50 ml). The toluene layer was washed with water (50 ml), dried over MgSO4 and concentrated in vacuo. The resulting residue was applied to column chromatography on silica gel. The column was eluted with hexane-AcOEt (8:1). The fractions containing the desired product were concentrated to afford 1.1 g of S,N-dimethyl-N'-nitro-N-trichloromethanesulfenylisothiourea as a pale yellow crystal, m.p. 75°-78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05256679 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-341e08c05c364c8098613c4433a8f977 |
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| Source note | uspto-grants-1993_10 |
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