HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethoxymethane → 3-(Methoxymethoxy)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethoxymethane | HCID 8020 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Methoxymethoxy)benzaldehyde | HCID 12273513 | — |
Reaction Steps
In a preferred embodiment of the invention, m-hydroxybenzaldehyde and dimethoxymethane are dissolved in methylene chloride and p-toluenesulfonic acid monohydrate is added. The mixture is refluxed overnight using a Soxhlet extractor containing type 3A molecular sieves, and the product, m-methoxymethoxybenzaldehyde, is isolated and purified by standard procedures. For example, after the reaction mixture cools, triethylamine is added to neutralize the acid catalyst and the mixture is washed with dilute sodium hydroxide solution and water, dried over sodium sulfate and evaporated. The residue is purified by distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03987105 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-990c1a175afc4bae82e86b792fcf5b6c |
| Source note | uspto-grants-1976_10 |