HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonic acid → p-(2-Acetamidoethyl)benzenesulphonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | N-(2-phenylethyl)acetamide | HCID 70143 | — |
| Product | p-(2-Acetamidoethyl)benzenesulphonyl chloride | HCID 3015782 | 45% |
Reaction Steps
N-Phenethylacetamide (4.50 g, 27.6 mmol) was added to sulfurochloridic acid (30 mL) slowly at 0-5° C. The resulting reaction mixture was stirred at room temperature for 2 h. The reaction mixture was poured into ice-water and stirred for 10 min. The mixture was extracted with DCM. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate and concentrated to afford the title compound as a brown solid (3.30 g, 12.64 mmol, 45% yield). MS (ESI) m/z 262.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156798B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-3f24ffb28f2141bbb946d7b287d56a41 |
| Source note | uspto-grants-2015_10 |