HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Acetoxy-3-methoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | o-Vanillin | HCID 8991 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 2-Acetoxy-3-methoxybenzaldehyde | HCID 251703 | — |
Reaction Steps
To a solution of o-vanillin (10.1 g) and a catalytic quantity (0.8 g) of dimethylaminopyridine in N-diisopropylethyl amine (23 mL) at 0° C. was added acetic anhydride (8 mL). The solution was stirred overnight, poured into 2N hydrochloric acid (100 mL), extracted with dichloromethane and the solvent removed in vacuo to afford a yellow solid. Recrystallization from ethanol yielded yellow crystals (10.9 g, 85%): m.p. 75.4-76.2° C., lit17 m.p. 76° C.; EIMS m/z 194 (M+), 152, 106, 43.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777578B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-6b9024bc3b2949aa9c629344e94e9e1a |
| Source note | uspto-grants-2004_08 |