HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-Benzyloxy-phenyl)-(3,5-dimethoxy-phenyl)-methanol → (3-Benzyloxyphenyl)-(3,5-dimethoxyphenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-Benzyloxy-phenyl)-(3,5-dimethoxy-phenyl)-methanol | HCID 69204493 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3-Benzyloxyphenyl)-(3,5-dimethoxyphenyl)methanone | HCID 69203059 | 93.1% |
Reaction Steps
To a stirred solution of (3-benzyloxy-phenyl)-(3,5-dimethoxy-phenyl)-methanol (11.51 g, 32.9 mmol) in CH2Cl2 (30 mL) at room temperature was added activated MnO2 powder (13.28 g, 153 mmol) and kept adding 2˜3 equivalents of MnO2 every 3˜5 h until HPLC showed disappearance of the starting material. The black suspension was filtered through a Celite pad, concentrated in vacuo to give (3-benzyloxy-phenyl)-(3,5-dimethoxy-phenyl)-methanone as a clear oil (10.67 g, 93% yield): 1H NMR (CDCl3) δ 3.82 (s, 6H, OCH3), 5.11 (s, 2H, CH2), 6.67 (t, J=2 Hz, 1H, Ar), 6.92 (d, J=2 Hz, 2H, Ar), 7.17-7.22 (m, 1H, Ar), 7.33-7.45 (m, 8H, Ar). The product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07470723B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-75cab3d8fe4b4749b6f9337804f5df78 |
| Source note | uspto-grants-2008_12 |