Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenyl isocyanate | HCID 7672 | — |
Reaction Steps
Carbon dioxide was added subsurface to a dichloromethane (20 mL) solution containing aniline (Ph--NH2) (0.02 mol, 1.86 g) and triethylamine (0.06 mol, 6.0 g) at -10° C. (ice and salt bath) for 40 min at a pressure of 0 psig. The reaction mixture was transferred rapidly via cannula under carbon dioxide to the precooled solution of phosphorus oxychloride (0.02 mol, 3.2 g) in 20 mL dichloromethane. After stirring for ca. 30 min at -10° C. a white ppt. formed. The ppt. was filtered off and the filtrate concentrated in vacuo. The residue was extracted with 3×20 mL diethyl ether. The ether layers were concentrated and the residue was distilled under vacuum (ca. 0.1-0.3 torr) collecting product, phenyl isocyanate, at 71°-73° C. (1.45 g, 61%) of 99% purity as judged by GC. IR (neat) 2266 cm-1. 1H NMR (CDCl3) δ 7.30 (t, 2H, J=7.8), 7.17 (t, 1H, J=7.5), 7.07 (d, 2H, J=6.7) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05189205 |
|---|
| Source dataset | uspto-grants-1993_02 |
|---|
| ORD ID | ord-a2b0fcbe9a3546a5a7dfd35be46eac46 |
|---|
| Source note | uspto-grants-1993_02 |
|---|