HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Cyanophenylboronic acid → tert-butyl 5-(3-cyanophenyl)-2H-1,4-oxazine-4(3H)-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Cyanophenylboronic acid | HCID 2734325 | — |
| Reactant | tert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylate | HCID 86680661 | — |
| Product | tert-butyl 5-(3-cyanophenyl)-2H-1,4-oxazine-4(3H)-carboxylate | HCID 86680665 | 63% |
Reaction Steps
This compound was prepared from tert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylate and 3-cyanophenylboronic acid using a procedure similar to that described in Example 2 (Steps 1-3a) above. The product was isolated as an off-white solid (63% yield); 1H-NMR (d6-DMSO) 1.08 (9H, s), 3.69 (2H, t), 4.12 (2H, t), 6.61 (1H, s), 7.50-7.52 (2H, m), 7.62-7.66 (2H, m); MS ES(+) 231.0 (M+-tBu). IR λmax=2225, 1697 cm−1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765751B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-4b49c24cc79542b08b13d7f7fb70596c |
| Source note | uspto-grants-2014_07 |