Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Catalyst | Triphenylphosphine Oxide | HCID 13097 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | Cyclohexyl isocyanate | HCID 18502 | 142.5% |
Reaction Steps
500 g of chlorobenzene and 7 g of triphenylphosphine oxide (0.025 mol) were placed in the glass vessel and 47 g of gaseous phosgene was introduced at room temperature. The reaction mixture was subsequently heated to 78° C., with vigorous phosgene reflux being established. While stirring vigorously at 78-80° C., a total of 99.2 g of cyclohexylamine (1 mol) dissolved in 200 g of chlorobenzene and at the same time a further 116 g of phosgene were introduced over a period of 3 hours. After addition was complete, the system was maintained at 78-80° C. for a further one hour without introduction of phosgene to allow further reaction to occur and the residual unreacted phosgene was subsequently stripped out at 40° C. by means of nitrogen. The reaction mixture obtained was a fluid suspension from which the solid obtained was separated by filtration. 1.9 g of solid were able to be isolated in this way. The filtered crude product was worked up by distillation. Removal of the solvent and fractional distillation gave 84.6 g of cyclohexyl isocyanate (0.677 mol). This corresponds to 67.7% of the theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07482481B2 |
|---|
| Source dataset | uspto-grants-2009_01 |
|---|
| ORD ID | ord-d4298122423f48bd8cd09ca0b02ff7b0 |
|---|
| Source note | uspto-grants-2009_01 |
|---|