HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrachloroethylene → Di-p-tolylcarbodiimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrachloroethylene | HCID 31373 | — |
| Reactant | 4-Methylphenyl isocyanate | HCID 69325 | — |
| Reactant | 1H-Phosphole, 2,3-dihydro-4-methyl-1-phenyl-, 1-oxide | HCID 69722 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Product | Di-p-tolylcarbodiimide | HCID 69763 | 77% |
Reaction Steps
p-Tolylisocyanate (150 parts) was stirred under a nitrogen atmosphere at 115° C with 2,2,2-diazabicyclo-octane equivalent to the acidity of the isocyanate (0.14 parts) and 1-phenyl-3-methyl-phospholene-1-oxide (0.75 parts of a 0.1% solution in perchloroethylene) an amount of 5 ppm on the isocyanate. After 8 hours, examination by infra-red showed all isocyanate groups to have disappeared. The red-brown single phase liquid was distilled in vacuo to give 96.2 parts (77% of theory) of di-p-tolylcarbodiimide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04085140 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-d56affcc338d4d87b1d39049214f4902 |
| Source note | uspto-grants-1978_04 |