HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorine monoxide → 2-(1-Chloroethyl)benzenesulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorine monoxide | HCID 24646 | — |
| Reactant | 2-Ethylbenzenesulfonyl chloride | HCID 2737373 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(1-Chloroethyl)benzenesulfonyl chloride | HCID 13364625 | 83.9% |
Reaction Steps
A solution of 2-ethylbenzenesulfonyl chloride (obtained by chlorosulfonation of ethylbenzene) (7.78 g) in carbon tetrachloride (5.0 ml) was contacted with a solution of dichlorine monoxide (82 mmol) in carbon tetrachloride (100 ml) and the mixture was heated in a closed system at 50°-60° for 16 hrs. The mixture was dried (MgSO4) and volatiles were removed under vacuum. The residue was kugelrohr distilled to give 7.63 g of colorless oil, bp 75°-80° (0.15 mm). 1H nmr δCDCl3TMS 8.20-7.35 (m). 6.13 (q, J=7 Hz), 1.90 (d, J=7 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04723990 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-5a26a82ee29e4183bd849568dc3c6a8f |
| Source note | uspto-grants-1988_02 |