Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl 3-methoxyacrylate | HCID 5323651 | — |
| Reactant | HCID 22897235 | HCID 22897235 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57440609 | HCID 57440609 | 83.2% |
Reaction Steps
To a solution of tert-butyl N-(2-formyl-3-methoxyphenyl)carbamate (7.8 g, 31 mmol) [described in Adv. Synth. Catal. 2003, 345, 743-765] and methyl trans-3-methoxyacrylate (7.4 mL, 68.4 mmol) dissolved in 150 ml of methanol, was added slowly 100 mL of an aqueous solution of hydrochloric acid 3M. The resulting mixture was stirred under reflux for 3 hours. The reaction mixture was then cooled to room temperature and neutralised by adding Na2CO3. The aqueous solution was extracted with CH2Cl2 (4×150 mL). The combined organic layers were dried over MgSO4, filtered and evaporated under vacuum. The crude product was then filtered on silica gel (AcOEt:cyclohexane/1:1) to afford 5.6 g of compound of molecular formula C12H11NO3. Aspect: yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07977354B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-0c96656498674307936e64d21f7dd9ab |
|---|
| Source note | uspto-grants-2011_07 |
|---|