HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655986Generated: October 30, 2026
4-Toluenesulfonyl chloride → HCID 178427424, compound
https://huagongshe.com/reaction/655986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 178509136 | HCID 178509136 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178427424 | HCID 178427424 | 48.4% |
Reaction Steps
To a solution of 5-phenyl-4H-1,2,4-triazol-3-amine (354 mg, 2 mmol) in dry pyridine (10 mL) was added 4-methylbenzenesulfonyl chloride (427 mg, 2.24 mmol). The solution was stirred at room temperature under Argon. After 48 h, the pyridine was removed in vacuo and flashed off with toluene. The residue was partitioned between CH2Cl2 and 1M NaOH. The organic phase was washed with 1M NaOH until no turbidity was observed on rectification of a small sample. The alkaline phase was made acidic (˜pH 3) with 1M HCl and extracted with CH2Cl2. After drying over Na2SO4, the solvent was removed in vacuo to give 0.41 g crude product. The crude product was dissolved hot EtOAc (16 mL), diluted with hexane (16 mL), and seeded to give fine white needles (304 mg) with mp 220-221° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071631B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-2124787c566f495a9d9038315810e943 |
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| Source note | uspto-grants-2011_12 |
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