HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dichlorobenzene → HCID 20465756, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dichlorobenzene | HCID 4685 | — |
| Reactant | Isocyanic acid | HCID 6347 | — |
| Reactant | 1-Methylnaphthalene | HCID 7002 | — |
| Reactant | Propylene Carbonate | HCID 7924 | — |
| Catalyst | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 20465756 | HCID 20465756 | 16% |
Reaction Steps
Some mixed solvents such as mixtures of propylene carbonate and toluene and mixtures of one or more organic carbonates with solvents such as xylene, toluene, benzene, chlorobenzene, dichlorobenzene, methylnaphthalene, and nitro hydrocarbons can be used effectively as solvents in the process of this invention. The process of this invention can be run at temperatures below 0 degrees C. using excess liquid HNCO as solvent. For instance, the reaction of alpha-terpinyl isocyanate with an excess of HNCO using CF3SO3H as catalyst at -20 degrees C. for 2 hours gave a 16% yield of menthane diisocyanate with a selectivity of 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04618707 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-4f5ebb6e8aa7498fa1ff27408707adae |
| Source note | uspto-grants-1986_10 |