HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Benzoxazines
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 4,4'-Dihydroxybiphenyl | HCID 7112 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Benzoxazines | HCID 17845026 | 292.5% |
Reaction Steps
To a flask of 0.5 L in volume, 71.7 g (0.77 mol) of aniline and 150 mL of dioxane were placed and the mixture was stirred to dissolve. Then, 37.3 g of a formaldehyde solution (a 36 to 38% aqueous solution) was added dropwise to be reacted at room temperature for 2 hours. Thereafter, 71.5 g (0.38 mol) of 4,4′-dihydroxybiphenyl was added to be reacted with stirring at 100 to 110° C. for 6 hours. After completion of the reaction, a precipitate was filtrated and dried in a vacuum drier at 95° C. for 8 hours to obtain 148 g of the compound (E-1) having at least two benzoxazine rings and represented by the formula (15) below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08470918B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-25ed945f6951465ab13793d3113fd1d9 |
| Source note | uspto-grants-2013_06 |