HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 24704709, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3'-Aminoacetophenone | HCID 7417 | — |
| Reactant | 1-Propanesulfonyl chloride | HCID 66279 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 24704709 | HCID 24704709 | 100.8% |
Reaction Steps
1 g (7.4 mmol) of 3-aminoacetophenone were dissolved in 35 ml of dry dichloromethane. To the resultant solution cooled at 0° C. 0.89 ml (11.09 mmol) of anhydrous pyridine and 1.26 g (8.87 mmol) of 1-propanesulfonic acid chloride were added. After stirring the reaction mixture for 20 h at room temperature and under inert atmosphere, 15 ml of water were added. The two layers were separated, and the aqueous layer was washed with 2×15 ml of dichloromethane. The organic layers were washed with 30 ml of water and dried over anhydrous sodium sulfate. The dichloromethane layer was evaporated to dryness to yield a yellow solid, 1.8 g (yield=100%) of N-(3-acetylphenyl)-1-propane-sulfonamide which was directly used for the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947688B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-076fece14880486fb6b837d51b779443 |
| Source note | uspto-grants-2011_05 |