HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 3-n-Butyl-5-(4-formylbenzylidene) hydantoin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-n-Butyl-5-[4-(1,3-dioxol-2-yl)benzylidene] hydantoin | HCID 54044432 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-n-Butyl-5-(4-formylbenzylidene) hydantoin | HCID 53793291 | — |
Reaction Steps
3-n-Butyl-5-[4-(1,3-dioxol-2-yl)benzylidene] hydantoin (2.7 g; 0.0085 mole) was dissolved in acetone (100 ml.) and stirred overnight at room temperature with p-toluene sulphonic acid (0.5 g.). The hazy solution was evaporated in vacuo and the resultant solid suspended in water (100 ml) and neutralised to pH 7 using dilute sodium bicarbonate solution. The residual solid was filtered off, washed with water and dried to give the title compound m.p. 180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04293563 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-4ff5eea0dfb64dcfa512b571882168fd |
| Source note | uspto-grants-1981_10 |