HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016402Generated: October 30, 2026
4-Toluenesulfonyl chloride → HCID 11438722, compound
https://huagongshe.com/reaction/1016402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3H-Pyrazol-3-one, 4-(1,1-dimethylethyl)-5-(hydroxymethyl)- | HCID 18406897 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11438722 | HCID 11438722 | 62.5% |
Reaction Steps
To a suspension of 4-tert-butyl-5-hydroxymethylpyrazol-3-one (6.25 g, 0.037 mol) in dry dichloromethane (200 ml) was added p-toluene sulfonyl chloride (9.8 g, 0.051 mol) followed by triethylamine (6.14 ml, 0.044 mol) dropwise. The solution was stirred at room temperature for 3 days. Dichloromethane (250 ml) was then added to dilute and the solution was washed with brine (250 ml), dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by silica gel chromatography with 0%→30% ethyl acetate/dichloromethane as eluent to give the title compound (7.5 g). Data for the title compound: 1H NMR (400 MHz, DMSO) δ 1.28 (9H, s), 2.43 (3H, s), 4.49 (2H, m), 5.32 (1H, m), 7.47 (2H, m), 7.86 (2H, m), 12.28 (1H, s); MS (ES+) m/e 325 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476030B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-59043d2841704686a7a20fde1fc5ecad |
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| Source note | uspto-grants-2002_11 |
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