HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Cyanide → Isophorone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Cyanide | HCID 768 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Isophorone | HCID 6544 | — |
| Reactant | Triethylmethylammonium methyl carbonate | HCID 11019667 | — |
| Product | Isophorone | HCID 6544 | — |
| Product | 3-Cyano-3,5,5-trimethylcyclohexanone | HCID 99068 | — |
Reaction Steps
To 622 g (4.5 mol) of isophorone in the presence of 4 g (0.021 mol) of triethylmethylammonium methylcarbonate there are added 288.3 g of a mixture of 3 mol of HCN and 1.5 mol of isophorone, over a period of 120 min and at a reaction temperature of 120° C. The HCN conversion at the end of the reaction is 99.9%. Following neutralization with 2.4g of H3PO4 the mixture is distilled. There are obtained 424.1 g of isophorone and 479.2 g of 3-cyano-3,5,5-trimethylcyclohexanone: the distillation residues weigh 12.8 g, this is equivalent to 1.4% based on the crude product used. The 3-cyano-3,5,5-trimethylcyclohexanone yield is thus 96.7% and the isophorone selectivity 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05516928 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-cc51bc8e6a6048aba97ac7bd7aacc511 |
| Source note | uspto-grants-1996_05 |