HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzoylbenzeneboronic acid → tert-butyl 5-(4-benzoylphenyl)-2H-1,4-oxazine-4(3H)-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzoylbenzeneboronic acid | HCID 4197235 | — |
| Reactant | tert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylate | HCID 86680661 | — |
| Product | tert-butyl 5-(4-benzoylphenyl)-2H-1,4-oxazine-4(3H)-carboxylate | HCID 86680674 | 65% |
Reaction Steps
This compound was prepared from tert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylate and 4-benzoylphenylboronic acid using a procedure similar to that described in Example 2 (Steps 1-3a) above. The product was isolated as a white solid (65% yield); 1H-NMR (d6-DMSO) 1.11 (9H, s), 3.71 (2H, t), 4.15 (2H, t), 6.65 (1H, s), 7.37-7.39 (2H, m), 7.57-7.59 (2H, m), 7.68-7.71 (5H, m); MS ES(+) 366.2 (M++1); Anal. Calcd for C22H23NO4: C, 72.31; H, 6.34; N, 3.83. Found: C, 71.95; H, 6.24; N, 9.98. IR λmax=1695, 1645, 1604, 1360 cm−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765751B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-2d915ef19ac548d384b69c9f4219f338 |
| Source note | uspto-grants-2014_07 |