HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-2-butanone → 2-Oxobutyl-thiacyclohexanium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-2-butanone | HCID 13156 | — |
| Reactant | Thiane | HCID 15367 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Oxobutyl-thiacyclohexanium bromide | HCID 85787952 | 72.7% |
Reaction Steps
In a 100 ml three-necked flask, 4 g of pentamethylene sulfide was dissolved in 40 ml of acetone. To the solution, 6 g of l-bromo-2-butanone was added dropwise while stirring. After leaving for 24 hours, the deposited white crystal was collected by filtration. The white crystal was ground to a powder, which was washed with ether. The powder was dried by a vacuum drier at 30° C. for six hours to obtain 7.2 g of 2-oxobutyl-thiacyclohexanium bromide (yield: 72.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06602647B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-029deade3c73470c9de10026eb530550 |
| Source note | uspto-grants-2003_08 |