HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Benzoate → Trimethyl orthoformate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Benzoate | HCID 7150 | — |
| Reactant | Tributylmethylammonium | HCID 36209 | — |
| Reactant | Tetramethyl orthocarbonate | HCID 74613 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Trimethyl orthoformate | HCID 9005 | — |
| Product | Benzaldehyde dimethyl acetal | HCID 62375 | — |
Reaction Steps
1062 g of tetramethoxymethane, 303 g of methyl benzoate, 225 g of 60% methyltributylammonium methosulfate solution and 910 g of methanol were electrolyzed at 3 A. The voltage per gap was kept below 5 V, the temperature was 30° C., and the pumping rate was 190 l/h. After the electrolysis had ended, 10.0 GC area % of trimethoxymethane and 13.2 GC area % of benzaldehyde dimethyl acetal had formed in the electrolyte; tetramethoxyethane had been degraded from 42.5% to 25.6 GC area %, and methyl benzoate was down to 0.4 GC area %, having been converted to more than 95%. Low-boiling byproducts included methyl formate at 2.2 GC area % in the electrolyte.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06822124B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-ad31c5d3274e413788fc678a432849b9 |
| Source note | uspto-grants-2004_11 |