HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181671Generated: October 30, 2026
Sodium Carbonate → Methyl 3-methyl-1-benzofuran-6-carboxylate
https://huagongshe.com/reaction/2181671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | Methyl 3-(allyloxy)-4-iodobenzoate | HCID 22481791 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Tetrabutylammonium chloride hydrate | HCID 16212273 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-methyl-1-benzofuran-6-carboxylate | HCID 22481752 | 67% |
Reaction Steps
Methyl 3-(allyloxy)-4-iodobenzoate (2.0 g, 6.28 mmol) is dissolved in DMF (15 ml), treated with Pd(OAc)2 (71 mg, 0.31 mmol), Na2CO3 (1.67 g, 15.7 mmol), sodium formate (427 mg, 6.28 mmol), and n-Bu4NCl.H2O (1.92 g, 6.92 mmol) and stirred at 80° C. for 2 days. The mixture is then filtered, the liquor is diluted with EtOAc (75 ml) and washed with 50% saturated NaCl (4×25 ml) followed by 5% HCl (25 ml). The organic layer is dried (Na2SO4), filtered, and concentrated to a brown oil. The crude material is chromatographed over 50 g slurry-packed silica gel, eluting with 20% EtOAc/hexane. The appropriate fractions are combined and concentrated to afford 797 mg (67%) of methyl 3-methyl-1-benzofuran-6-carboxylate as a pale oil. HRMS (FAB) calcd for C11H10O3+H: 191.0708, found 191.0714 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06894042B2 |
|---|
| Source dataset | uspto-grants-2005_05 |
|---|
| ORD ID | ord-aad4a5cd9e014d83a0ae4bdefd50e538 |
|---|
| Source note | uspto-grants-2005_05 |
|---|