HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → Benzenesulfonyl Bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Benzenesulfinic acid, sodium salt | HCID 2723840 | — |
| Product | Benzenesulfonyl Bromide | HCID 11138664 | — |
Reaction Steps
Benzenesulfonyl bromide was synthesized with 1316.0 g of the mother liquid containing sodium benzenesulfinate by procedures similar to those of the fourth step and the fifth step of Example 1 except that bromine was used instead of chlorine in the fifth step. Thus, 36.0 g of benzenesulfonyl bromide was yielded. Gas chromatographic analysis revealed that the concentration of benzenesulfonyl bromide in the organic layer was 81.3% (weight; 29.27 g, 0.133 mole), and the yield was 94.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07507812B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-18aca290182c4aa0a2257fc9e441bb3d |
| Source note | uspto-grants-2009_03 |