HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → 2,3-Dihydro-2,2-dimethyl-7-benzofuranol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3-Dihydro-2,2-dimethyl-7-benzofuranol | HCID 15278 | — |
| Product | 7-Methoxy-2,2-dimethyl-2,3-dihydro-1-benzofuran | HCID 13531377 | — |
Reaction Steps
The starting material 2,3-dihydro-2,2-dimethyl-7-benzofuranol is prepared from catechol and 3-chloro-2-methylpropene as described by Neth. No. 6,500,340. The material (16.4 g) is added to 125 ml of water and contacted with 8 ml of 50% NaOH. After stirring one-half hour, 16.4 g of dimethylsulfate is added and the resulting suspension is stirred and heated at 60° for 2 hours. The resulting mixture is extracted with methylene chloride. The organic phase is dried over sodium sulfate and the solvent is evaporated under reduced pressure. The residual oil is distilled to afford 2,3-dihydro-2,2-dimethyl-7-methoxybenzofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04576632 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-cde4ca8fb730469395b1c40d09defc1a |
| Source note | uspto-grants-1986_03 |