HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 21521118, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Reactant | 2-Phenyl-1,3,4-oxadiazol-2-IN-5-one | HCID 352208 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21521118 | HCID 21521118 | — |
Reaction Steps
40.5 g of 5-phenyl-1,3,4-oxadiazol-2-one (0.25 mol), 51.5 g of 2,6-di-tert.-butyl-phenol (0.25 mol), 8.2 g of paraformaldehyde (0.27 mol) and 0.7 g of hexamethylenetetramine in 150 ml of dimethylformamide and 15 ml of water are heated to 110°C for 15 hours, whilst stirring. A yellowish solution results, from which the 3-(3,5-di-tert.-butyl-4-hydroxybenzyl)-5-phenyl-1,3,4-oxadiazol-2-one (stabiliser No. 1) which is formed crystallises out on cooling to room temperature. The product is filtered off, washed with a little methanol and dried in vacuo at 70°C. Melting point: 164°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03971803 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-ec8fb97a6ca84cfe96774e2fc2e5ed02 |
| Source note | uspto-grants-1976_07 |