HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-2-cyclopropyl methoxy-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Cyclopropanemethanol | HCID 75644 | — |
| Reactant | 7-Chloro-2-[(E)-2-(3-oxiranyl-phenyl)-vinyl]-quinoline | HCID 86720731 | — |
| Product | 2-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-2-cyclopropyl methoxy-ethanol | HCID 86720735 | 40.5% |
Reaction Steps
To a solution of epoxide 30 (3.0 g, 0.0098 mol) in dichloromethane (30.0 ml) was added cyclopropyl methanol (60.0 ml) at ambient condition and stirred for 5 minutes. To the above solution was added boron trifluoride-ethyl ether complex (3.0 ml, 0.0238 mol) slowly at such a rate so as to maintain the temperature of reaction between 25° C. to 30° C. The reaction was stirred at ambient temperature for 18 hours. A saturated aqueous solution of sodium carbonate (3.0 g) was added carefully and the resulting mixture was extracted with dichloromethane (30 ml). The organic phase was separated followed by usual workup and FC to give ether-alcohol 44 (1.5 g, 40.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09102665B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-5a15d3ce1f644f92af85239b98d01a9a |
| Source note | uspto-grants-2015_08 |