HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Phenoxyphenyl)boronic acid → HCID 86680676, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Phenoxyphenyl)boronic acid | HCID 2773559 | — |
| Reactant | tert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylate | HCID 86680661 | — |
| Product | HCID 86680676 | HCID 86680676 | 25% |
Reaction Steps
This compound was prepared from tert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylate and 2-phenoxyphenylboronic acid using a procedure similar to that described in Example 2 (Steps 1-3a) above. The product was isolated as a white solid (25% yield); 1H-NMR (d6-DMSO) 1.07 (9H, s), 3.09 (2H, m), 3.97 (2H, m), 6.19 (1H, s), 6.78 (2H, m), 6.97-7.04 (2H, m), 7.15-7.19 (1H, m), 7.26-7.32 (4H, m); MS ES(+) 298.0 (M+-tBu). IR λmax=1692 cm−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765751B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-526c4d388f524dfcb948d51fd1509935 |
| Source note | uspto-grants-2014_07 |