HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811028Generated: October 27, 2026
Formaldehyde → 6-bromo-5-methyl-3-phenyl-2H-benzo[e][1,3]oxazin-4(3H)-one
https://huagongshe.com/reaction/1811028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 3-bromo-6-hydroxy-2-methyl-N-phenylbenzamide | HCID 59374988 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 6-bromo-5-methyl-3-phenyl-2H-benzo[e][1,3]oxazin-4(3H)-one | HCID 59375051 | 60% |
Reaction Steps
A mixture of 3-bromo-6-hydroxy-2-methyl-N-phenylbenzamide (Intermediate 16-1, 40 mg, 0.131 mmol) and paraformaldehyde (11.77 mg, 0.392 mmol) in TFA (1 mL) was heated at 100° C. for 4 h. The TFA was removed under vacuum, and the residue was diluted with EtOAc (80 mL), washed with NaHCO3 (aq) (10 mL), water (10 mL) and brine (10 mL), and dried and concentrated. The residue was purified by column chromatogaphy (eluting with a gradient from 95:5 to 70:30 hexane-EtOAc) to give 6-bromo-5-methyl-3-phenyl-2H-benzo[e][1,3]oxazin-4(3H)-one (25 mg, 45%). 1H NMR (400 MHz, chloroform-d) δ 7.63 (1 H, d, J=8.80 Hz), 7.37-7.50 (3 H, m), 7.29-7.35 (2 H, m), 6.81 (1 H, d, J=8.80 Hz), 5.48 (2 H, s), 2.80 (3 H, s). Mass spectrum m/z 318, 320 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362065B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-8ba3afde7b3d4e0baf4dcbc57594180c |
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| Source note | uspto-grants-2013_01 |
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