HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896891Generated: October 29, 2026
Benzenesulfonyl chloride → HCID 689074, compound
https://huagongshe.com/reaction/896891
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | HCID 689074 | HCID 689074 | — |
Reaction Steps
To benzenesulfonyl chloride (0.5 mL, 3.92 mmol) in 4:1 v/v tetrahydrofuran—water (20 mL) was added powdered zinc (282 mg, 4.31 mmol, 1.1 eq.) followed by 4-bromophenacyl bromide (1.31 g, 4.70 mmol, 1.2 eq.). The reaction mixture was stirred at room temperature for 17 hours. The volatile solvent was evaporated under reduced pressure and poured into water. The reaction was extracted with ethyl acetate (2×150 mL), and the combined organic layers were washed with brine (1×100 mL), dried (MgSO4), filtered, and evaporated under reduce pressure. The crude product was purified using MPLC (Biotage) eluted with 5:1 v/v hexane-ethyl acetate. Crystallization from dichloromethane-hexane gave the desired product as a white fluffy solid (486 mg, 36.6% yield). MS LC-MS (ES MH+=340); TLC (Rf=0.30, 25% ethyl acetate-hexane)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06919371B2 |
|---|
| Source dataset | uspto-grants-2005_07 |
|---|
| ORD ID | ord-058adeb4ff214bfc932bbb1c3e6f82e3 |
|---|
| Source note | uspto-grants-2005_07 |
|---|