HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 3-(Benzyloxy)-4-methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Reactant | [3-(Benzyloxy)-4-methylphenyl]methanol | HCID 24721056 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-(Benzyloxy)-4-methylbenzaldehyde | HCID 16101389 | — |
Reaction Steps
To a solution of (3-(benzyloxy)-4-methylphenyl)methanol (entire amount) in DMSO (15 mL) was added 2-iodoxybenzoic acid (3.20 g), and the mixture was stirred at room temperature for 2 hr. Ethyl acetate (250 mL) was added to the reaction mixture, and the insoluble material was filtered off. The filtrate was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.50 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181186B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-08b4b0578b36493d9c7e9fbb0b8faf73 |
| Source note | uspto-grants-2015_11 |