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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615438Generated: October 31, 2026

4-Phenoxyphenylboronic acid → HCID 86680675, compound

https://huagongshe.com/reaction/1615438

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactanttert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylateHCID 86680661—
ProductHCID 86680675HCID 8668067550%

Reaction Steps

This compound was prepared from tert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylate and 4-phenoxyphenylboronic acid using a procedure similar to that described in Example 2 (Steps 1-3a) above. The product was isolated as a white solid (50% yield); 1H-NMR (d6-DMSO) 1.24 (9H, s), 3.68 (2H, t), 4.09 (2H, t), 6.38 (1H, s), 6.96-6.98 (4H, m), 7.11 (1H, m), 7.21 (2H, d), 7.37 (2H, t); MS ES(+) 298.1 (M+-tBu). IR λmax=1697 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765751B2
Source datasetuspto-grants-2014_07
ORD IDord-adb15e05db69497788eced5d6a9f8b65
Source noteuspto-grants-2014_07