HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865799Generated: October 25, 2026
Thionylchloride water → 3,4,5-Trifluorobenzenesulfonyl chloride
https://huagongshe.com/reaction/1865799
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionylchloride water | HCID 86607486 | — |
| Reactant | 3,4,5-Trifluorodiazobenzene | HCID 86607487 | — |
| Product | 3,4,5-Trifluorobenzenesulfonyl chloride | HCID 2778858 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629341B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-e3a9a01706564daa8dca64e4cae27bc4 |
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| Source note | uspto-grants-2009_12 |
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