HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250277Generated: October 26, 2026
Toluene → 5-(4-Hydroxy-2-methyl-phenyl)-benzofuran-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/250277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Ethyl (5-bromobenzofuran)-2-carboxylate | HCID 735184 | — |
| Reactant | 2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol | HCID 51358338 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-Dicyclohexylphosphino-2,6-dimethoxybiphenyl | HCID 66545337 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(4-Hydroxy-2-methyl-phenyl)-benzofuran-2-carboxylic acid ethyl ester | HCID 67271576 | 56% |
Reaction Steps
A solution of 5-bromo-benzofuran-2-carboxylic acid ethyl ester (275 mg, 1.02 mmol) and 2-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenol (239 mg, 1.11 mmol) in toluene (5.0 mL) and THF (5.0 mL) is added to a flask. The flask is evacuated and re-filled with N2 three times. Pd(OAc)2 (5 mg, 0.022 mmol) and 2-dicyclohexylphosphino-2,6-dimethoxy-1,1′-biphenyl (20 mg, 0.049) and potassium phosphate, tribasic, N-hydrate (432 mg, 2.04 mmol) are added and the mixture is heated at 85° C. for 8 hours. The reaction mixture is cooled to room temperature and filtered through a pad of diatomaceous earth. The filtrate is concentrated to a residue which is purified by silica gel chromatography eluting with 20-30% EtOAc/Hexanes to provide the title compound (179 mg, 56%). ES/MS m/e 297.0 (M+1), 295.0 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07863302B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-aa7bed7c608a4062abad4592f270c584 |
|---|
| Source note | uspto-grants-2011_01 |
|---|