HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 19881348, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | HCID 178515948 | HCID 178515948 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19881348 | HCID 19881348 | — |
Reaction Steps
To a suspension of 20.1 g (0.05 mol) diselenosalicylic acid in 20 ml water is added 15.0 g (0.375 mol) sodium hydroxide in one portion with stirring. After dissolution 39.75 g (0.375 mol) sodium carbonate and 23.9 g (0.1375 mol) sodium dithionite are added and the mixture is heated to reflux for 2 h, allowed to cool to room temperature and 30.1 g (0.1625 mol) 4-methylbenzyl bromide in 125 ml ethanol is added dropwise within 15 minutes, followed by stirring overnight. The reaction mixture is acidified under stirring with 150 ml aqueous hydrochloric acid (32%), the white precipitate is filtered off, washed with 200 ml water and dried. The residue is purified by recrystallization from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05141955 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-5a89bb4d7f5b405e99a80632c2104ea4 |
| Source note | uspto-grants-1992_08 |