HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 6-(4-Fluorophenyl)-2,3-dihydroimidazo[2,1-b][1,3]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4,5-Dihydro-2-thiazolamine | HCID 15689 | — |
| Reactant | 2-Chloro-4'-fluoroacetophenone | HCID 120248 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(4-Fluorophenyl)-2,3-dihydroimidazo[2,1-b][1,3]thiazole | HCID 13639897 | 99% |
Reaction Steps
A mixture of 51.6 g (0.3 mol) of 4-fluorophenacylchloride, 33.66 g (0.33 mol) of 2-aminothiazoline and 200 ml of ethanol was heated at reflux for 2 hours. The mixture was cooled to room temperature at which point 300 ml of water was added. After a reflux period of 2 hours, the mixture was concentrated to remove about 190 ml of aqueous alcohol. The pH of the residue was adjusted to about 2 with 10% hydrochloric acid (10 ml). The solid product was separated and dried to give 65.4 g (85%) of 6-(4-fluorophenyl)-2,3-dihydroimidazo[2,1-b]thiazole, m.p. 116-118°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05008390 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-f58c4174469045b382dca4fb2bbeb62a |
| Source note | uspto-grants-1991_04 |