HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 3-(3-cyanophenyl)-5-(dimethoxymethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Methyl 3-(3-cyanophenyl)-5-(formyl)benzoate | HCID 9795280 | — |
| Reactant | Methylorthoformate | HCID 53629101 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-(3-cyanophenyl)-5-(dimethoxymethyl)benzoate | HCID 9839713 | — |
Reaction Steps
In 200 ml of methanol, were dissolved 2.00 g of the compound obtained in Example 11, 0.86 ml of methyl orthoformate and 0.004 g of p-toluenesulfonic acid monohydrate. The resulting solution was refluxed for 12 hours. After completing the reaction, 0.03 ml of triethylamine was added to the reaction solution, and the solvent was then removed under reduced pressure. Ethyl acetate was added to the residue, and the resulting solution was extracted with ethyl acetate. The organic layer was dried over sodium sulfate. The solvent was removed under reduced pressure to provide 2.35 g (quantitatively) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06538137B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-8891fa78ae5b408290049a3f33f94012 |
| Source note | uspto-grants-2003_03 |