HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → N,N-diethyl-2-nitrobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Reactant | Diethylammonium chloride | HCID 10197650 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N-diethyl-2-nitrobenzenesulfonamide | HCID 4229519 | 79.2% |
Reaction Steps
To a solution of 132.6 g of o-nitrobenzenesulfonyl chloride in 700 ml of tetrahydrofuran was added 88.5 g of diethylamine at 5°-15°. The reaction mixture was stirred at room temperature for 1 hour before the precipitated diethylamine hydrochloride was removed by filtration. The filtrate was evaporated to dryness in-vacuo and the residue dissolved in 1-chlorobutane. The 1-chlorobutane solution was washed with water, dried over magnesium sulfate and evaporated in-vacuo to give 122.4 g of o-nitro-N,N-diethylbenzenesulfonamide as a dark oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04293330 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-d58875a01e36460ea4df9c3969887d28 |
| Source note | uspto-grants-1981_10 |