HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Alcohol → 3-(Allyloxycarbonyl)methylimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 3-Ethoxycarbonylmethylimidazo[5,1-b]thiazole | HCID 19605065 | — |
| Product | 3-(Allyloxycarbonyl)methylimidazo[5,1-b]thiazole | HCID 19605012 | — |
Reaction Steps
A 30 mg potion of a sodium ethoxide powder was added to 6.2 ml of an allyl alcohol solution containing 314.2 mg of 3-ethoxycarbonylmethylimidazo[5,1-b]thiazole, and the mixture was then was then heated under reflux for 7 hours. After cooled, the reaction solution was concentrated under reduced pressure, and the organic layer extracted with dichloromethane (10 ml×4) was dried over anhydrous magnesium sulfate, and then filtered, and the solvent was evaporated under reduced pressure. The resulting crude product was purified by a silica gel column chromatograph to obtain 240.4 mg of the title compound as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990101 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-bcc09a9dffdc4d64a4f4c2988d62cb07 |
| Source note | uspto-grants-1999_11 |