HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 20524789, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 20524745 | HCID 20524745 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20524789 | HCID 20524789 | — |
Reaction Steps
A mixture of N-(2-oxopropyl)-4'-chloromethanesulphonanilide (6.0 g), ethane-1,2-diol (10 ml), 4-toluenesulphonic acid (0.1 g) and toluene (75 ml) was stirred and boiled under reflux with water separation by means of a Dean and Stark receiver. After 3 hours the reaction mixture was cooled and poured into water (about 200 ml) containing a few drops of sodium hydroxide solution. The organic layer was separated, washed with water, dried (MgSO4) and evaporated to a brown oil, which gave fawn coloured crystals from a solution in toluene/80°-100° petrol. Yield 6.0 g (86%). Melting point 84°-85°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04309559 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-7e1570929e514708b5b8de24da4d9158 |
| Source note | uspto-grants-1982_01 |