HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 53784400, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 54231039 | HCID 54231039 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53784400 | HCID 53784400 | — |
Reaction Steps
25.5 g (0.1 mol) of ethyl 3-(4-aminobenzenesulfonyl) acrylate, prepared by refluxing 3-(4-aminobenzenesulfonyl)acrylamide in an excess of absolute ethanol and in the presence of concentrated sulfuric acid as a condensing agent, are dissolved in acetone (100 ml). 14.5 ml of triethylamine (0.1 mol) are added as an HCl acceptor. A solution of p-toluenesulfonyl chloride (19.1 g, 0.1 mol) in 50 ml acetone is added dropwise at room temperature. The reaction mixture is left for 12 hours and is then poured into ice water. The precipitated solid is recovered by filtration, dried and recrystallized from ethanol, giving ethyl 3-[4-(4-methylbenzenesulfonamido)benzenesulfonyl]acrylate: ##SPC15##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03943154 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-97dbb4cf405b4d5989daf047fd52a477 |
| Source note | uspto-grants-1976_03 |