HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3,4-Dimethoxy-2,5-bis(methoxymethoxy)-6-methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Bromo-3,4-dimethoxy-2,5-bis(methoxymethoxy)-6-methylbenzene | HCID 12721542 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3,4-Dimethoxy-2,5-bis(methoxymethoxy)-6-methylbenzaldehyde | HCID 14180320 | 80% |
Reaction Steps
To a cold solution of 2,3-dimethoxy-5-methyl-1,4-bismethoxymethyloxy-6-bromobenzene [oily substance, δ 2.34 (3H), 3.57 (3H), 3.64 (3H), 3.84 (6H), 5.01 (2H), 5.09 (2H)] (9.00 g, 25.6 mmol) in absolute ether (90 ml) was added a solution of 15% n-butyllithium in hexane (17.6 ml). The mixture was stirred for 30 minutes. Dimethylformamide (9.36 g, 128 mmol) was added and the reaction was continued under the same conditions for 30 minutes. Working up in a conventional manner gave 2,3-dimethoxy-5-methyl-1,4-bismethoxymethyloxy-6-formylbenzene [oily substance, δ2.48 (3H), 3.55 (3H), 3.58 (3H), 3.85 (3H), 3.95 (3H), 4.99 (2H), 5.13 (2H)]. Yield 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04751303 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-2558b084a773483b9adcc8a559cca122 |
| Source note | uspto-grants-1988_06 |