HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Methyl Benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Ethanol | HCID 702 | — |
| Product | Methyl Benzoate | HCID 7150 | — |
Reaction Steps
Substantially the same procedure as in Example 7 was repeated, except that the activated catalyst prepared in Example 4 was used, that benzaldehyde was used instead of the methacrolein, and that ethanol was used instead of the methanol, to thereby effect a reaction for producing methyl benzoate. Analysis was made with respect to the reaction mixture which was withdrawn from the outlet of the reactor 10 hours after the start of the reaction. As a result, it was found that the conversion of benzaldehyde was 76.2%, and the selectivity for methyl benzoate was 93.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06040472 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-578ba19c00c84f64afc4666439de70a1 |
| Source note | uspto-grants-2000_03 |