HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929598Generated: October 31, 2026
Potassium Carbonate → HCID 86718778, compound
https://huagongshe.com/reaction/929598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4-Dichlorobenzeneboronic acid | HCID 2734330 | — |
| Reactant | HCID 86718777 | HCID 86718777 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 86718778 | HCID 86718778 | 54.4% |
Reaction Steps
A mixture of 8-bromo-3-(tert-butyl)-3,4-dihydro-2H-benzo[e][1,3]oxazine (0.46 g, 1.71 mmol), potassium carbonate (0.945 g, 4.0 equiv), 3,4-dichlorophenylboronic acid (0.489 g, 1.5 equiv), and tetrakis(triphenylphosphine)Pd (0) (63 mg, 3.2 mol %) was heated at 53-64° C. for 3 hours, then at 80-87° C. for 2.5 hours. To the mixture was added additional 3,4-dichlorophenylboronic acid (0.2 g) and the resulting mixture was heated at 80-87° C. overnight. Upon cooling to room temperature, the reaction mixture was concentrated. The crude product was purified by column chromatography to give 3-(tert-butyl)-8-(3,4-dichlorophenyl)-3,4-dihydro-2H-benzo[e][1,3]oxazine (0.313 g) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296696B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-2e9585fe5f9b46c2b17c02c8a48e1e3b |
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| Source note | uspto-grants-2016_03 |
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