HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(3-Methylbutoxy)benzene-1-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium 4-(3-methylbutoxy)benzenesulfonate | HCID 23701366 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-Methylbutoxy)benzene-1-sulfonyl chloride | HCID 18324001 | — |
Reaction Steps
A mixture of sodium 4-(3-methylbutoxy)benzenesulfonate (2.5 grams, 9.4 mmole), thionyl chloride (10 mL), and 5 drops of N,N-dimethylformamide was heated at reflux for 5 hours. After cooling, the excess thionyl chloride was evaporated and the residue was taken up in ethyl acetate. The solution was cooled in an ice bath and water was added. The organic phase was separated and washed with water and brine. After drying over sodium sulfate, the solvent was evaporated to afford the title compound as an oil, 2.34 grams (95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06087392 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-7d57581e5cfc4751a6676bd51867cbd1 |
| Source note | uspto-grants-2000_07 |