Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-Fluorophenyl)acetic acid | HCID 9837 | — |
| Reactant | 3,5-Dimethoxybenzaldehyde | HCID 81747 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 57703495 | HCID 57703495 | 82.87% |
Reaction Steps
A mixture of 4-fluorophenyl acetic acid (0.928 g, 6.02 mmol), 3,5 dimethoxybenzaldehyde (1 g, 6.02 mmole), Ac2O (1 ml) and triethylamine (0.5 ml) was heated at 100° C. for 12 hours. Upon completion (as monitored by TLC using hexane-ethyl acetate (3:2), the reaction mixture was cooled to room temperature and concentrated HCL (5 ml) was added. The precipitate was dissolved in CH2Cl2 (100 ml), washed with 10% aqueous NaOH (3×50 ml) and the basic solution was acidified (PH-1) with concentrated HCL. After stirring, the precipitate was collected and dried to get the product (1.5 g, 82.87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08263044B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-a780e0ca3e2f4a808a1d63bc87d7ddc9 |
|---|
| Source note | uspto-grants-2012_09 |
|---|