HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 22474170, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethylenethiourea | HCID 2723650 | — |
| Reactant | 1-(1-Benzothiophen-2-yl)-2-bromoethan-1-one | HCID 2795258 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 22474170 | HCID 22474170 | 75.6% |
Reaction Steps
A mixture of 1-(benzo[b]thiophen-2-yl)-2-bromoethan-1-one (21.96 g), 2-imidazolidinethione (7.81 g) and ethanol (300 ml) was heated under reflux for 10 minutes. Acetic acid (150 ml) was added, then the mixture was heated under reflux for 18 hours and allowed to cool to ambient temperature. The resulting solid was collected by filtration, washed with ethanol (50 ml) and ether (50 ml), then dried in vacuo at 100° C. for 3 hours to give 3-(benzo[b]thiophen-2-yl)-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide (19.6 g) as a light brown solid, m.p. 275-285° C. (decomposes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900216B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-3b12617c00734856bfe4e0e0734ef99f |
| Source note | uspto-grants-2005_05 |