HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385637Generated: November 1, 2026
Methylhydrazine → N,4-dimethylbenzenesulfonohydrazide
https://huagongshe.com/reaction/1385637
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,4-dimethylbenzenesulfonohydrazide | HCID 280433 | 95% |
Reaction Steps
Into a 100 mL three necked round bottom flask equipped with a mechanical stirrer, thermometer, and dropping funnel under an atmosphere of nitrogen was added THF (25 mL), methylhydrazine (2.53 g, 2.92 mL, 55 mmol), and triethylamine (4.35 g, 5.99 mL, 55 mmol). The temperature of the mixture was lowered to approximately 5° C. and 4-methylbenzenesulfonyl chloride (9.5 g, 50 mmol) dissolved in 25 mL of THF was added dropwise at a rate such that the temperature did not rise over 10° C. The cooling bath was removed and the mixture was allowed to stir overnight at RT. Ether (100 mL) was added to the reaction mixture and the resulting slurry was washed with water (50 mL), brine (50 mL), dried (Na2SO4), and the solvent was removed in vacuo to give 9.5 g (95% yield) of the title product. 1H NMR (CDCl3) δ 7.7 (d, 2H), 7.4 (d, 2H), 3.6 (s, b, 2H), 2.8 (s, 3H), 2.4 (s, 3H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06262305B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-3441e79c14e7458faf15310c55ba3692 |
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| Source note | uspto-grants-2001_07 |
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