HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dichlorobenzenesulfonyl chloride → HCID 11045855, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dichlorobenzenesulfonyl chloride | HCID 79401 | — |
| Reactant | Resorcinol, 5-methyl-, monohydrate | HCID 3083941 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 11045855 | HCID 11045855 | — |
Reaction Steps
Orcinol monohydrate (1.42 g, 10.0 mmol) and 2,5-dichlorobenzenesulfonyl chloride (2.46 g, 10.0 mmol) were mixed in saturated aqueous NaHCO3 (30 mL) and diethyl ether (30 mL). The biphasic mixture was stirred vigorously at ambient temperature overnight. The reaction mixture was diluted with water (50 mL) and extracted into ethyl acetate (3×50 mL). The organic phase was washed with brine (2×50 mL) and dried over Na2SO4. After removing the solvent in vacuo, the residue was purified by flash column chromatography (dichloromethane to 2% ethyl acetate in dichloromethane) to give the title compound as apale yellow solid (1.65 g, 51%). 1H-NMR (300 MHz, CDCl3) δ 7.95 (s, 1H), 7.55 (s, 2H), 6.56 (s, 2H), 6.46 (s, 1H), 5.29 (s, 1H), 2.25 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891909 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-19f3a214cb8840c786a2d8e375ec6f46 |
| Source note | uspto-grants-1999_04 |