HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Benzoyl-2-nitrobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | [3-(Dimethoxymethyl)-4-nitrophenyl]phenylmethanone | HCID 19816024 | — |
| Solvent | Methyl Chloride | HCID 6327 | — |
| Product | 5-Benzoyl-2-nitrobenzaldehyde | HCID 19816055 | — |
Reaction Steps
A mixture of (3-dimethoxymethyl-4-nitro-phenyl)-phenyl-methanone (0.0659 mol) and 5N HCl (40 mL) in CH3Cl (80 mL) was stirred at room temperature overnight. Then the mixture was refluxed for 4 h. After cooling, the organic layer was separated. The organic layer was alkalized by adding dropwise NH4OH. The organic layer was washed with water, dried (MgSO4) and evaporated. The residue (14.6 g) was crystallized from diisopropyl ether/EtOAc (50 mL:20 mL). The precipitate was filtered off, washed with diisopropyl ether/EtOAc, diisopropyl ether and dried in vacuo at 50° C. to yield the title compound as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383637B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-b2f38c0dbe6d4b08a1b80c443b2dd8d8 |
| Source note | uspto-grants-2013_02 |