HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-(2-Chloroethoxy)ethoxy)ethanol → HCID 10095388, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-(2-Chloroethoxy)ethoxy)ethanol | HCID 78871 | — |
| Reactant | 3-Butyryl-4-(2-methylphenylamino)8-hydroxyquinoline | HCID 10403732 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10095388 | HCID 10095388 | 68.4% |
Reaction Steps
A mixture of 3-butyryl-4-(2-methylphenylamino)-8-hydroxyquinoline (2.40 g, 7.5 mmol), potassium t-butoxide (1.22 g, 10 mmol) and 2-(2-(2-(chloroethoxy)ethoxy)ethanol (2.18 ml, 15 mmol) in tetrahydrofuran (40 ml) was heated at reflux for 3 days. The solvent was evaporated, the residue taken up in dichloromethane, washed with water and brine, dried and evaporated. Chromatography (silica gel, 0-10% methanol in ethyl acetate) and crystallisation from ether gave 3-butyryl-4-(2-methylphenylamino)-8-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)quinoline (2.32 g, 68%) as a hygroscopic solid, m.p. 102°-104°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05432182 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-20f74809e27449aeb95a4968a96d5786 |
| Source note | uspto-grants-1995_07 |