HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxybenzaldehyde → (2-Methoxyphenyl)(3-methyl-2-methoxymethoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxybenzaldehyde | HCID 8658 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(Methoxymethoxy)-2-methylbenzene | HCID 3839351 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (2-Methoxyphenyl)(3-methyl-2-methoxymethoxyphenyl)methanol | HCID 19812676 | 137.2% |
Reaction Steps
1-Methyl-2-methoxymethoxybenzene (15.2 g) was added to a mixture of 75 ml of a 1.6M solution of n-butyl lithium in hexane and 18.1 ml of tetramethylethylenediamine at 0° C. with stirring. After 4 hours, 13.6 g of o-anisaldehyde dissolved in 30 ml of tetrahydrofuran was added. The mixture was allowed to react for 0.5 hour and was then poured into a mixture of ice and saturated aqueous ammonium chloride. The resulting mixture was extracted with ether and the ether extract was dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain 39.5 g of the title compound as an off-white solid. The assigned structure was consistent with the proton NMR spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05071465 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-9405cc635e3c4ef996944285c3b2a2e4 |
| Source note | uspto-grants-1991_12 |