HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 10-(2-Ethylhexyloxy)decanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,10-Decanediol | HCID 37153 | — |
| Reactant | 2-Ethylhexyl bromide | HCID 86804 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 10-(2-Ethylhexyloxy)decanol | HCID 19694647 | 72.1% |
Reaction Steps
A 1-liter flask equipped with a stirrer and distiller was charged with 25 g (0.14 mol) of 1,10-decanediol, 8.09 g (0.14 mol) of KOH and 300 ml of xylene, and the resultant mixture was heated at 120° C. for 1 hour, thereby distilling off water formed. To this reaction mixture, were added 23.1 g (0.12 mol) of 2-ethylhexyl bromide, and the resulting mixture was heated and stirred for 15 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and washed with water. After the solvent was distilled off under reduced pressure, the resulting residue was purified by column chromatography on silica gel, thereby obtaining 24.8 g (yield: 72%) of 10-(2-ethylhexyloxy)decanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05723497 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-31b708e4b55e4146a82a5bb5a9af3de8 |
| Source note | uspto-grants-1998_03 |