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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016402Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 11438722, compound

https://huagongshe.com/reaction/1016402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant3H-Pyrazol-3-one, 4-(1,1-dimethylethyl)-5-(hydroxymethyl)-HCID 18406897—
SolventDichloromethaneHCID 6344—
ProductHCID 11438722HCID 1143872262.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476030B1
Source datasetuspto-grants-2002_11
ORD IDord-59043d2841704686a7a20fde1fc5ecad
Source noteuspto-grants-2002_11