HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → [4-(7-Oxido-3-phenyl-1,7-naphthyridin-2-yl)phenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | [4-(3-Phenyl-1,7-naphthyridin-2-yl)phenyl]methanol | HCID 59846130 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | [4-(7-Oxido-3-phenyl-1,7-naphthyridin-2-yl)phenyl]methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910561B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-f3e426e616924cc5a4059ced2e349ddb |
| Source note | uspto-grants-2011_03 |