HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Benzenesulfonamide, 3-chloro-N-2-propynyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Chlorobenzenesulphonyl chloride | HCID 17909 | — |
| Reactant | Propargylamine | HCID 239041 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzenesulfonamide, 3-chloro-N-2-propynyl- | HCID 14157397 | 95.8% |
Reaction Steps
Sodium hydroxide (0.60 g, 15 mmol) was dissolved in 10 ml of water and this solution was added to 0.66 g of propargylamine (12 mmol). Under ice-cooling, 2.11 g of 3-chlorobenzenesulfonyl chloride (10 mmol) was added dropwise to the mixture. The reaction temperature was raised again to room temperature and the mixture was stirred for 3 hours. The reaction mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, and concentrated to obtain N-propargyl-3-chlorobenzenesulfonamide (2.20 g). NMR spectrum of this product was as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04749407 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-3ec96eed15d34dd6984162ca1f114eb5 |
| Source note | uspto-grants-1988_06 |