HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 8-bromo-3,6-di-tert-butyl-3,4-dihydro-2H-benzo[e][1,3]oxazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 2-Bromo-4-tert-butylphenol | HCID 75147 | — |
| Product | 8-bromo-3,6-di-tert-butyl-3,4-dihydro-2H-benzo[e][1,3]oxazine | HCID 86718559 | 85% |
Reaction Steps
A mixture of paraformaldehyde (19.99 g, 0.666 mol) and tert-butylamine (70.26 mL, 0.666 mol) in isopropanol (260 mL) was heated to gentle reflux under nitrogen for 75 minutes. A solution of 2-bromo-4-(tert-butyl)phenol (30.5 g, 0.133 mol) in isopropanol (40 mL) was then added and the mixture refluxed for a further 20 hours. The cooled reaction mixture was then concentrated to afford a yellow solid. The crude product was re-crystallized from methanol (100 mL) to give 8-bromo-3,6-di-tert-butyl-3,4-dihydro-2H-benzo[e][1,3]oxazine (36.74 g, 85% yield) as a cream crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409893B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-e6f4493f6a2043f28e181fd0b05e5bf5 |
| Source note | uspto-grants-2016_08 |