HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-1-[1-(4-Chlorophenyl)cyclobutyl]ethanone → 1-[1-(4-Chlorophenyl)cyclobutyl]-2-(3,4,5,6-tetrahydropyrimidin-2-ylthio)ethanone hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-1-[1-(4-Chlorophenyl)cyclobutyl]ethanone | HCID 21901921 | — |
| Reactant | HCID 178527864 | HCID 178527864 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-[1-(4-Chlorophenyl)cyclobutyl]-2-(3,4,5,6-tetrahydropyrimidin-2-ylthio)ethanone hydrobromide | HCID 21258364 | 86% |
Reaction Steps
A solution of 2-bromo-1-[1-(4-chlorophenyl)cyclobutyl]ethanone (2.9 g) in acetone (25 ml) was added to a solution of 3,4,5,6-tetrahydropyrimidine-2-thiol (1.2 g) in acetone (150 ml), then the mixture was heated under reflux for 1 hour, and allowed to cool to ambient temperature. The resulting solid was collected by filtration and dried in vacuo at ambient temperature to give 1-[1-(4-chlorophenyl)cyclobutyl]-2-(3,4,5,6-tetrahydropyrimidin-2-ylthio)ethanone hydrobromide as a white solid (3.5 g), m.p. 205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06187802B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-b2703ce6696c44799f310dd2f2dbb392 |
| Source note | uspto-grants-2001_02 |