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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605006Generated: October 27, 2026

m-Chloroperbenzoic acid → [4-(7-Oxido-3-phenyl-1,7-naphthyridin-2-yl)phenyl]methanol

https://huagongshe.com/reaction/605006

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant[4-(3-Phenyl-1,7-naphthyridin-2-yl)phenyl]methanolHCID 59846130—
SolventChloroformHCID 6212—
Product[4-(7-Oxido-3-phenyl-1,7-naphthyridin-2-yl)phenyl]methanolHCID 59846139—

Reaction Steps

To a solution of [4-(3-phenyl-1,7-naphthyridin-2-yl)phenyl]methanol (142 mg, 0.455 mmol) in chloroform (3 mL) was added a solution of m-chloroperbenzoic acid (85%, 105 mg, 0.47 mmol) in chloroform (2 mL). The reaction was stirred over night and then the solvent was removed in vacuo. The residue was digested with diethyl ether twice to remove the m-chlorobenzoic acid and give the title compound as a yellow solid. 1H-NMR (500 MHz, CDCl3): δ 9.07 (1H, s), 8.24 (1H, d, J=6.8 Hz), 8.09 (1H, s), 7.70 (1H, d, J=7.1 Hz), 7.41 (2H, d, J=8.1 Hz), 7.22-7.39 (7H, m), 4.71 (2H, s). m/e (m+1): 329.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910561B2
Source datasetuspto-grants-2011_03
ORD IDord-f3e426e616924cc5a4059ced2e349ddb
Source noteuspto-grants-2011_03