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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615437Generated: October 31, 2026

4-Benzoylbenzeneboronic acid → tert-butyl 5-(4-benzoylphenyl)-2H-1,4-oxazine-4(3H)-carboxylate

https://huagongshe.com/reaction/1615437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzoylbenzeneboronic acidHCID 4197235—
Reactanttert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylateHCID 86680661—
Producttert-butyl 5-(4-benzoylphenyl)-2H-1,4-oxazine-4(3H)-carboxylateHCID 8668067465%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765751B2
Source datasetuspto-grants-2014_07
ORD IDord-2d915ef19ac548d384b69c9f4219f338
Source noteuspto-grants-2014_07