HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → Benzylbenzene diisocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Diethanolamine | HCID 8113 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzylbenzene diisocyanate | HCID 19824838 | — |
Reaction Steps
The above amounts of diethanolamine and iodine were added to the above amount of soybean oil with stirring. The mixture was stirred for 22 hours at a temperature between about 180° F. and about 228° F. Then, the above amounts of maleic anhydride, toluene and p-toluenesulphonic acid were added with stirring. The mixture was refluxed for 10 hours using a Dean-Stark distilling trap, then distilled out of solvent to give a liquid soybean oil based polyol with a hydroxyl number of 54. A reaction mixture of about 10.00 grams of the polyol and the above indicated amount of diphenylmethane diisocyanate yielded a solid soybean oil based polyurethane material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541536B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-2073206467494843b9a58b69b4b418bf |
| Source note | uspto-grants-2013_09 |