Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063Generated: October 27, 2026

4-Toluenesulfonyl chloride → 1H-Imidazole-4-methanol, 1-[(4-methylphenyl)sulfonyl]-

https://huagongshe.com/reaction/2063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantHCID 178418488HCID 178418488—
SolventDichloromethaneHCID 6344—
Product1H-Imidazole-4-methanol, 1-[(4-methylphenyl)sulfonyl]-HCID 1152894680%

Reaction Steps

4-Hydroxymethylimidazole hydrochloride (10 g) was suspended in dichloromethane (200 ml). ρ-Toluenesulfonyl chloride (15.58 g) was added and triethylamine (25.8 ml) was added dropwise to the stirred reaction mixture which was allowed to stir at room temperature overnight. The mixture was washed with water (2×100 ml) and brine (1×100 ml) and the organic layer was dried and evaporated to leave a clear oil which was recrystallised from ethyl acetate/hexane to afford the title compound as a white crystalline solid (15 g, 80%). 1H NMR (360 MHz, CDCl3) δ2.44 (3H, s), 4.55 (2H, s), 7.21 (1H, s), 7.35 (2H, d, J=8.0 Hz), 7.62 (2H, d, J=8.0 Hz 7.98 (1H, s). MS (CI+) m/z 253 (M+H, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728695
Source datasetuspto-grants-1998_03
ORD IDord-3a8bce93f6c044b885e4e50a87273179
Source noteuspto-grants-1998_03