HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266533Generated: October 31, 2026
4-Chloro-2-toluidine → HCID 54103172, compound
https://huagongshe.com/reaction/266533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-2-toluidine | HCID 7251 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 54103172 | HCID 54103172 | 908.2% |
Reaction Steps
t-Butyl nitrite (1.52 g) was added to a mixture of 4-chloro-2-methylaniline (2.0 g) and dimethyl disulphide (14.49 g) in chloroform. The mixture was heated to 70° C. to initiate the reaction. A solution of 4-chloro-2-methylaniline (9.0 g) in chloroform and t-butyl nitrite (7.25 g) were added simultaneously while maintaining the temperature in the range 60°-70° C. Further dimethyl disulphide (11.83 g) was added followed by the simultaneous addition of a solution of 4-chloro-2-methylaniline (9.0 g) in chloroform and t-butyl nitrite (7.25 g) while maintaining the temperature in the range 50°-55° C. The mixture was stirred at room temperature for 2 hours. It was washed thoroughly with water, 2M hydrochloric acid, water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give 5-chloro-2-(methylsulphenyl)toluene (22.15 g) as a red oil which was not further characterized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650533 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-80af69d270c54662a39ca96a80688b1b |
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| Source note | uspto-grants-1997_07 |
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