HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 86718774, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | (1,1'-Biphenyl)-2-ol | HCID 7017 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86718774 | HCID 86718774 | — |
Reaction Steps
To a mixture of 2-phenylphenol (17.0 g, 0.1 mol) and paraformaldehyde (15.0 g, 0.5 mol) in isopropanol (100 mL) was added tert-butylamine (36.5 g, 0.5 mol) dropwise. The resulting reaction mixture was refluxed under nitrogen overnight. The cooled reaction mixture was then concentrated under reduced pressure to give a yellow oil. The yellow oil was dissolved in ethyl acetate to form a solution which was washed with water, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford 3-(tert-butyl)-8-phenyl-3,4-dihydro-2H-benzo[e][1,3]oxazine (30 g) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296696B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-2a77b3548a014ec58325af13ef510187 |
| Source note | uspto-grants-2016_03 |