Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3',4'-Dimethoxycinnamic acid | HCID 16848 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | Methyl 3,4-dimethoxycinnamate | HCID 94307 | 80% |
Reaction Steps
To a suspension of 3-(3,4-dimethoxyphenyl)-2-propenoic acid (21.8 g, 105 mmol) in methanol (220 ml) was added thionyl chloride (23.0 mL, 315 mmol) under ice cooling and the mixture was stirred at 60° C. for 12 hours. The resulting mixture was concentrated under reduced pressure, and the residue was added to water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate, water and saturated aqueous sodium chloride, and dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was crystallized from ethyl acetate-hexane to obtain 18.7 g (yield 80%) of the title compound. mp. 72–74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07208495B2 |
|---|
| Source dataset | uspto-grants-2007_04 |
|---|
| ORD ID | ord-b82b9fe6b0b34087a1915e45f917ac45 |
|---|
| Source note | uspto-grants-2007_04 |
|---|