HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Ethoxyphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Ethoxyphenol | HCID 66755 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Ethoxyphenol | HCID 66755 | — |
| Product | 2-Ethoxy-4-prop-2-enylphenol | HCID 601250 | — |
Reaction Steps
To 34 ml of water were added in order 3.36 g of sodium hydroxide, 11.60 g of o-ethoxyphenol, 0.716 g of cupric chloride (CuCl2.2H2O; catalyst) and 7.07 g of allyl chloride. The reaction took place at 83° C and with stirring, for 3 hours. The reaction solution was then neutralized with hydrochloric acid and extracted with five portions of 30 ml of ether. The resulting ethereal extract was distilled to give 4.51 g of the desired o-ethoxy-p-allylphenol and 0.78 g of the unreacted o-ethoxyphenol. There was also obtained 6.56 g of by-product 1-allyloxy-2-ethoxybenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04048236 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-eac0ec537b37442292b1075a2dc7bb1d |
| Source note | uspto-grants-1977_09 |