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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252248Generated: October 29, 2026

Chlorosulfonic acid → 4-(4-methyl-oxazol-5-yl)-benzenesulfonyl Chloride

https://huagongshe.com/reaction/252248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantOxazole, 4-methyl-5-phenyl-HCID 594392—
SolventChloroformHCID 6212—
Product4-(4-methyl-oxazol-5-yl)-benzenesulfonyl ChlorideHCID 59788543—

Reaction Conditions

Temperature4 °C

Reaction Steps

To a chilled solution (ice-bath) of 4-methyl-5-phenyl-oxazole (0.2 g, 1.3 mmol) in CHCl3 (1 ml) was added drop-wise chlorosulfonic acid (0.5 ml, 7.7 mmol). The dark-brown reaction mixture was stirred at 4° C. for 30 min and slowly warmed to reflux. After 2 h the reaction mixture was poured into ice-water and extracted with ethyl acetate (3×). The combined organic extracts were washed with water, brine, dried (MgSO4.2H2O), filtered and evaporated to yield a light-brown solid: 0.19 g, (56%), MS: m/e 257.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868030B2
Source datasetuspto-grants-2011_01
ORD IDord-c652ab7c0f88496fa3853ee12ea694a5
Source noteuspto-grants-2011_01