HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 4-Cyclobutyl-1,3-thiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Bromo-1-cyclobutylethan-1-one | HCID 11062940 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Cyclobutyl-1,3-thiazol-2-amine | HCID 22063634 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
Thiourea (2.3 g, 30.0 mmol) was dissolved in ethanol (100 ml), added with 2-bromo-1-cyclobutyl-1-ethanone synthesized in the same manner as in Example 1, (E), and then heated to 100° C. The reaction solution was stirred for 1 hour, then returned to room temperature, neutralized with saturated sodium hydrogencarbonate and extracted with chloroform. The collected organic layer was washed with saturated brine, dried over magnesium sulfate and then concentrated under reduced pressure. The title compound was obtained as the residue without purification as a brown oily substance (5.4 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07056917B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-e8187ae78d1c4a36845fb1374412f289 |
| Source note | uspto-grants-2006_06 |