HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → m-Bromophenyl 3-methyl-2-butenyl sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Butene, 1-bromo-3-methyl- | HCID 70092 | — |
| Reactant | m-Bromobenzenethiol | HCID 80597 | — |
| Solvent | Water | HCID 962 | — |
| Product | m-Bromophenyl 3-methyl-2-butenyl sulfide | HCID 22640690 | — |
Reaction Steps
25.00 g (132.0 mmol) of 3-bromothiophenol, 200 ml of DMF and 18.23 g (138.0 mmol) of potassium carbonate are introduced into a three-necked flask. 18.0 ml (157.0 mmol) of 1-bromo-3-methyl-2-butene are added dropwise and the mixture is stirred at room temperature for five hours. The reaction medium is poured into water and extracted with ethyl acetate, and the organic phase is separated out after settling has taken place, washed with water, dried over magnesium sulphate and evaporated. 33.00 g (97%) of the expected compound are collected in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148245B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-0431190da25d4435a220758f831c06ff |
| Source note | uspto-grants-2006_12 |