HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829075Generated: November 1, 2026
4-Methoxybenzoic Acid → HCID 21030126, compound
https://huagongshe.com/reaction/1829075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzoic Acid | HCID 7478 | — |
| Reactant | Butyl Acrylate | HCID 8846 | — |
| Catalyst | Cupric acetate monohydrate | HCID 165397 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21030126 | HCID 21030126 | — |
Reaction Steps
A mixture of 4-methoxybenzoic acid (1.52 g, 10.0 mmol), palladium (II) acetate (0.56 g, 2.5 mmol), copper (II) acetate monohydrate (0.499 g, 2.5 mmol) and 4 Å molecular sieves (1.75 g) in DMF (40 ml) was stirred at room temperature for 5 minutes. Butyl acrylate was add (2.57 g, 20.0 mmol), and the resulting mixture was heated at 120° C. for 25 hours and then at 140° C. for 9 hours. Upon cooling the mixture was filtered and partitioned between dilute HCl aqueous solution and EtOAc. The organic layer was washed with saturated NaHCO3 aqueous solution, water, brine, then dried with anhydrous Na2SO4 and rotary evaporated to a brown oil. The oil was triturated with hexane and the remaining oil was chromatographed through silica gel column (20% to 30% EtOAc/Hexane gradient) to give the desired product contaminated with 4-methoxybenzoic acid. The mixture was dissolved in EtOAc and washed with saturated NaHCO3 aqueous solution, brine, dried with anhydrous Na2SO4. Removal of the solvent yielded butyl (6-methoxy-3-oxo-1,3-dihydro-2-benzofuran-1-yl)acetate as a light yellow oil (0.26 g, 9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07060844B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-ab72d27dc90942e18b2b51df5990555d |
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| Source note | uspto-grants-2006_06 |
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