HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013561Generated: October 25, 2026
Water → 2,3-Dihydrobenzofuran-5-sulfonyl Chloride
https://huagongshe.com/reaction/1013561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Dihydrobenzofuran | HCID 10329 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2,3-Dihydrobenzofuran-5-sulfonyl Chloride | HCID 2776154 | 100% |
Reaction Steps
3.56 g (29.6 mmol) 2,3-dihydrobenzofuran was added to a slurry of 5.44 g (35.5 mmol) sulfur trioxide-N,N-dimethylformamide complex in 12 mL 1,2-dichloroethane under argon. The reaction was heated to 85° C. for 1 hour and then cooled to room temperature. Thionyl chloride (2.6 mL, 35.5 mmol, 1.2 eq) was added dropwise and the reaction was slowly heated over the course of one hour, by which time it had reached 75° C. The mixture was allowed to cool to room temperature and 100 mL of methylene chloride and 100 mL water were added. The organic extract was separated, dried over magnesium sulfate filtered and evaporated to afford 6.56 g (100%) of 2,3-dihydrobenzofuran-5-sulfonyl chloride as a tan oil. (TLC Rf chloroform/hexanes=1/1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07981929B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-b5a5ddfa943a48ef87cc8d226139e9f9 |
|---|
| Source note | uspto-grants-2011_07 |
|---|