HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248558Generated: October 30, 2026
Methyl iodide → 1-Methoxymethyloxy-2,3,4,5-tetramethoxybenzene
https://huagongshe.com/reaction/248558
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methoxymethyloxy-4,5,6-trimethoxyphenol | HCID 20095709 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Methoxymethyloxy-2,3,4,5-tetramethoxybenzene | HCID 13495532 | — |
Reaction Steps
11.5 g of 2-methoxymethyloxy-4,5,6-trimethoxyphenol prepared in Referential Example 12 and 23.0 g of potassium carbonate were suspended in 100 ml of DMF. The suspension was heated at 45° C. while stirring, and 5.2 ml of iodomethane was dropwise added thereto. After the completion of the dropwise addition, the mixture was heated for 30 min, cooled and separated by filtration. 1 l of water was added to the mother liquor, and the mixture was extracted with ethyl acetate. The organic phase was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (eluent; n-hexane : ethyl acetate=85 : 15) to prepare 6.2 g of the product compound as a colorless oleaginous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05210239 |
|---|
| Source dataset | uspto-grants-1993_05 |
|---|
| ORD ID | ord-e0a1f68cf8774c448a93bebdd1f00271 |
|---|
| Source note | uspto-grants-1993_05 |
|---|