HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Toluene 2,4-Diisocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | 2,4-Diaminotoluene | HCID 7261 | — |
| Reactant | 2-Methyl-5-Nitroaniline | HCID 7444 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Product | Toluene 2,4-Diisocyanate | HCID 11443 | — |
Reaction Steps
250 g of the following mixture were introduced into a 0.7 liter autoclave: 2×10-3 % by weight of PdCl2, 4% by weight of FeOCl, 14.8% by weight of a bis-urea of 2,4-diamino toluene and 2-amino-4-nitrotoluene and 81% by weight of ethanol. The nitro groups of the urea used are oxidizing agents for the oxycarbonylation of the urea function. 120 bar of carbon monoxide were forced in at room temperature. The mixture was allowed to react for two hours at 180° C. The bis-urea was converted quantitatively. The bis-urethane of 2,4-diisocyanatotoluene was obtained with a selectivity of 50 mol % in addition to 10 mol % of isomeric aminourethanes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04304922 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-6aa5440d67bb4c6180faee262f866adb |
| Source note | uspto-grants-1981_12 |