HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dihydrobenzofuran → 2,3-Dihydrobenzofuran-5-sulfonyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dihydrobenzofuran | HCID 10329 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Product | 2,3-Dihydrobenzofuran-5-sulfonyl Chloride | HCID 2776154 | 30.2% |
Reaction Steps
2,3-dihydrobenzofuran (6.0 g, 49.94 mmol) is added over 20 minutes to chlorosulfonic acid (29.09 g, 249.69 mmol) at -20° C. The reaction mixture is quenched by addition of ice followed by water (20 mL). The mixture is then extracted with ethyl acetate. The combined organic estracts are washed with brine, dried (Na2SO4), and the solvent is evaporated. The crude product is purified by silica gel chromatography (30% ethyl acetate/hexane) to give 2,3-dihydrobenzofuran-5-sulfonyl chloride (3.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05455258 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-cb8419eb67094748a96a0fd327e9a9a8 |
| Source note | uspto-grants-1995_10 |