HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → methyl (E)-beta-methoxy-2-methylcinnamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Product | methyl (E)-beta-methoxy-2-methylcinnamate | HCID 86749647 | 94% |
Reaction Steps
A mixture of 1280 g (6.7 mol) of methyl 2-methylbenzoyl acetate, 848 g (8.0 mol) of trimethyl orthoformate, 400 ml of methanol and 10 ml of concentrated H2SO4 is stirred at room temperature for 12 h. The mixture is subsequently neutralized with 20 ml of pyridine and then concentrated, and the residue is fractionally distilled (boiling point 120°-123° C./0.6 torr). 1300 g (94%) of methyl (E)-β-methoxy-2-methylcinnamate are obtained as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05538940 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-7409648fc1e54629bcc22e1d32b6781b |
| Source note | uspto-grants-1996_07 |