HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184140Generated: October 27, 2026
Water → 2-Fluoro-4,5-dimethoxybenzene-1-sulfonyl chloride
https://huagongshe.com/reaction/2184140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Fluoro-1,2-dimethoxybenzene | HCID 593640 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-Fluoro-4,5-dimethoxybenzene-1-sulfonyl chloride | HCID 16785004 | — |
Reaction Steps
To a suspension of sulfur trioxide N,N-dimethylformamide complex (4.108 g, 27 mmol) in 1,2-dichloroethane was added 4-fluoroveratrole (30.49 g, 22 mmol) dropwise. The mixture was slowly heated to 85° C. in an oil bath. After 2.5 h, the solids had dissolved to afford a golden yellow solution. A trace of starting material was still present and heating was continued for a further 4.5 h. The oil bath was removed and thionyl chloride (1.95 mL, 27 mmol) added dropwise. The mixture was heated 4 h at 85° C. and allowed to cool to room temperature. The solution was poured into water and extracted with dichloromethane (3×50 mL), the combined organics washed with water, dried over magnesium sulfate and evaporated. Remaining traces of N,N-dimethylformamide were removed azeotropically with toluene to afford the product as an off-white solid that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900227B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-52f2a1d6a9ed4545ba3d122a895c9c45 |
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| Source note | uspto-grants-2005_05 |
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