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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553199Generated: October 25, 2026

Thionylchloride water → 3,4,5-Trifluorobenzenesulfonyl chloride

https://huagongshe.com/reaction/553199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionylchloride waterHCID 86607486—
Reactant3,4,5-TrifluorodiazobenzeneHCID 86607487—
Product3,4,5-Trifluorobenzenesulfonyl chlorideHCID 277885883%

Reaction Conditions

Temperature-10 °C

Reaction Steps

The flask containing the SOCl2/H2O solution is cooled again to −10° C. and a catalytic amount of Cu(I)Cl (˜50 mg) was added. The solution turns dark green in color. The flask was fitted with a 500 mL addition funnel (previously chilled to 0° C.) and the 3,4,5-trifluorodiazobenzene solution was quickly transferred to the funnel. The solution was immediately added dropwise over a period of 3 min. After addition, the reaction mixture slowly turns darker green in color, but after stirring for 5 min becomes bright, lime green. The reaction was stirred for an additional hour while warming to room temperature. The reaction mixture was transferred to a separatory funnel and extracted with CH2Cl2 (3×200 mL). The organic phases are combined and dried over anhydrous Na2SO4, filtered, and concentrated to give a dark-bronze oil (79.5 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951972B2
Source datasetuspto-grants-2011_05
ORD IDord-3dc833aa8c0e40679c779e1a0a7fa6e8
Source noteuspto-grants-2011_05