HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 4-(4-Chlorothiophen-2-yl)-1,3-thiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Acetyl-4-chlorothiophene | HCID 11105655 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4-Chlorothiophen-2-yl)-1,3-thiazol-2-amine | HCID 23030678 | — |
Reaction Steps
Bromine was added to an ether solution of 4-chloro-2-acetylthiophene under ice cooling, and the mixture was stirred at room temperature for 2 hours to obtain a brominated compound. Thiourea was added to an EtOH solution of the brominated compound at room temperature, and the mixture was stirred overnight at 80° C. to obtain 2-amino-4-(4-chlorothiophen-2-yl)thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361658B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-f5d94976bd19497ea4eb7126179aad9f |
| Source note | uspto-grants-2008_04 |