HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → N-[2-(furan-2-yl)ethyl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 2-(Furan-2-yl)ethan-1-amine | HCID 1132863 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-[2-(furan-2-yl)ethyl]benzenesulfonamide | HCID 53667225 | — |
Reaction Steps
3.2 g of 2-(2-aminoethyl)-furan are dissolved in 45 ml of pyridine and at 5° C. a solution of 8.8 g of benzenesulphonic acid chloride in 50 ml of pyridine is added. The resulting mixture is then stirred overnight at ambient temperature, the reaction product is evaporated down, the residue is taken up in water and extracted with methylene chloride. After the organic phase has been dried over magnesium sulphate the solution is concentrated by evaporation and chromatographed over a silica gel column using ethylene chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04870076 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-cf5f3aa3f3474a35a39da982a5f02528 |
| Source note | uspto-grants-1989_09 |