HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-Chloro-5-methoxyphenyl)methanol → 3-Chloro-5-methoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-Chloro-5-methoxyphenyl)methanol | HCID 12909342 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Chloro-5-methoxybenzaldehyde | HCID 21904633 | 77.1% |
Reaction Steps
A mixture of 3-chloro-5-methoxybenzyl alcohol (5.0 g, 28.9 mmol) and pyridinium chlorochromate (20% on alumina, 40 g, 37.8 mmol) was allowed to stir for 1.25 hr. Diethyl ether (200 ml) was then added followed by filtration of precipitate. The filtrate was concentrated under reduced pressure and the resulting residue was purified via silica gel chromatography using 40% dichloromethane, 60% petroleum ether as eluant, to give 3.8 g of 3-chloro-5-methoxybenzaldehyde. 1H-NMR (CDCl3): 3.84 (s, 3H) 7.13 (s, 1H), 7.28 (s, 1H), 7.41 (s, 1H), 9.89 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372873B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-c9aabc7581f849409c3bf1ca26d9fefe |
| Source note | uspto-grants-2013_02 |