HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrogallol → 4-(3,5-Dimethoxy-benzyloxy)-2-ethoxy-benzo[1,3]dioxole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrogallol | HCID 1057 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 2-Ethoxy-benzo[1,3]dioxol-4-ol | HCID 13447063 | — |
| Reactant | 1-(Bromomethyl)-2,4-dimethoxybenzene | HCID 15151907 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(3,5-Dimethoxy-benzyloxy)-2-ethoxy-benzo[1,3]dioxole | HCID 22000665 | — |
Reaction Steps
2-Ethoxy-benzo[1,3]dioxol-4-ol (1.11 g, 6.08 mmol), 4-bromomethyl-1,3-dimethoxybenzene (1.17 g, 5.08 mmol), potassium carbonate (0.77 g, 5.59 mmol) and 18-crown-6-ether (0.13 g, 0.51 mmol) were stirred together at room temperature in acetone (40 cm3, 99%) under nitrogen for 18 hours. The solution was evaporated under reduced pressure, and the residue was taken up in dichloromethane (30 cm3) and water (30 cm3). The aqueous layer was extracted with dichloromethane (3×30 cm3), and the combined extracts were washed with water (2×50 cm3), dried (MgSO4), and evaporated under reduced pressure. The residue was chromatographed (SiO2, dichloromethane) to give the di protected pyrogallol, (1.56 g, 92%) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06225352B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-644d4b1f7098443785983ae2a6c8536d |
| Source note | uspto-grants-2001_05 |