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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615439Generated: October 29, 2026

(2-Phenoxyphenyl)boronic acid → HCID 86680676, compound

https://huagongshe.com/reaction/1615439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Phenoxyphenyl)boronic acidHCID 2773559—
Reactanttert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylateHCID 86680661—
ProductHCID 86680676HCID 8668067625%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765751B2
Source datasetuspto-grants-2014_07
ORD IDord-526c4d388f524dfcb948d51fd1509935
Source noteuspto-grants-2014_07