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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494363Generated: October 30, 2026

Thionyl Chloride → HCID 59804979, compound

https://huagongshe.com/reaction/494363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 59804977HCID 59804977—
CatalystDimethylformamideHCID 6228—
ProductHCID 59804979HCID 59804979—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of thionyl chloride (3.0 mL) and 2 drops of DMF stirring under nitrogen at 0° C. is added the title B compound, 4-(5-methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-ylmethoxy)-benzenesulfonic acid sodium salt (1.1 g, 2.53 mmol) in one portion. The resulting suspension is stirred at 0° C. for 10 min. The ice bath is removed and the suspension is stirred at RT for 3 h. The solution is concentrated and the resulting residue is azeotrophed twice with toluene. The residue is taken up into DCM, filtered and evaporated at reduced pressure to give 4-[5-methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-benzenesulfonic acid chloride as an oil. It is used as such without any additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538135B2
Source datasetuspto-grants-2009_05
ORD IDord-a33bbcbb5852400f8fdee12e5a0a4202
Source noteuspto-grants-2009_05