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
The synthesis was carried out under radiation from a yellow lamp. A 100-millilitter three-port flask was prepared. Using the flask, 4 grams of pentamethylenesulfide was dissolved in 40 milli-litter of acetone. 6 grams of 1-bromo-2-butanone was dropped into the solution over agitation. After 24 hours, white crystal was precipitated, and was filtrated. The white crystal was pulverized, and the pulverized white crystal was washed in ether. The resultant crystal was dried by using a low-pressure drier at 30 degrees in centigrade for six hours. Then, 7.2 grams of 2-oxobutyl-thiacyclohexanium bromide was obtained. The yield was 72.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06638685B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-0566b95d821a4fccafa2c812b7f7b987 |
| Source note | uspto-grants-2003_10 |