HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(1-Hydroxyhexyl)-phenoxymethyl-oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-(1-Hydroxyhexyl)phenol | HCID 11790084 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(1-Hydroxyhexyl)-phenoxymethyl-oxirane | HCID 19829491 | — |
Reaction Steps
19.4 g. (0.1 mole) 3-(1-hydroxyhexyl)-phenol and 28.6 g. epichlorohydrin are dissolved in 25 ml. ethanol and heated to the boil. A solution of 6.6 g. potassium hydroxide in 3 ml. water and 25 ml. ethanol is then added dropwise thereto in the course of 15 minutes. The reaction mixture is boiled under reflux for 2 hours, the solvent is then distilled off and the residue is taken up in water. Extraction is carried out with ethyl acetate, the ethyl acetate phase is washed twice with aqueous sodium hydroxide solution and water, dried and evaporated to give 22.4 g. (89% of theory) of the title compound in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05025028 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-ac2c1377d029427d99d7036aacca91b8 |
| Source note | uspto-grants-1991_06 |