HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425586Generated: October 28, 2026
Diethyl Ether → Methyl 2-ethoxy-4-(1-hydroxy-2-methylpropan-2-yl)benzoate
https://huagongshe.com/reaction/2425586
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67244628 | HCID 67244628 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-ethoxy-4-(1-hydroxy-2-methylpropan-2-yl)benzoate | HCID 53412311 | 48% |
| Product | HCID 67244628 | HCID 67244628 | — |
Reaction Steps
Triethylamine (3.5 mL, 25.1 mmol) was added to a solution 2-ethoxy-4-(2-hydroxy-1,1-dimethylethyl)iodobenzene (4.0 g, 12.5 mmol) in methanol (20 mL) under an atmosphere of nitrogen. The reaction was purged twice with carbon monoxide, and palladium (II) acetate (0.2 g, 0.9 mmol) was added. The reaction was stirred at 80° C. for 18 h under a positive pressure of carbon monoxide. The reaction was diluted with ether, washed with 10% hydrochloric acid, aqueous sodium bicarbonate, brine, dried over anhydrous magnesium sulfate and concentrated. Purification of the crude residue by flash chromatography over silica gel using 20-75% ethyl acetate in hexanes gave methyl 2-ethoxy-4-(2-hydroxy-1,1-dimethylethyl)benzoate (1.5 g, 48%) as a yellow oil and 0.91 g of unreacted 2-ethoxy-4-(2-hydroxy-1,1-dimethylethyl)iodobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07964724B2 |
|---|
| Source dataset | uspto-grants-2011_06 |
|---|
| ORD ID | ord-bd290047cb9644e0b28fcc4ddda7df94 |
|---|
| Source note | uspto-grants-2011_06 |
|---|