HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → m-Bromophenyl 3-methyl-2-butenyl sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Butene, 1-bromo-3-methyl- | HCID 70092 | — |
| Reactant | m-Bromobenzenethiol | HCID 80597 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | m-Bromophenyl 3-methyl-2-butenyl sulfide | HCID 22640690 | — |
Reaction Steps
A solution of 3-bromothiophenol (5.0 g) in 60 mL of DMF was treated with 3.75 g of ground potassium carbonate and 3.2 mL of 3,3-dimethylallyl bromide. The reaction mixture was stirred at room temperature for two hours, poured onto 75 mL of ice-water, acidified to pH 2.0 with 10% HCl and extracted with three 75 mL portions of ether. The organic phase was dried over MgSO4, filtered and concentrated in vacuo to give a yellow oil. The product was purified by short path distillation (T=170° C. at 950 mTorr) to give 5.651 g of 1-bromo-3-(3-methyl-but-2-enylsulfanyl)-benzene as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354931B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-707df612164e4f529073e39112236676 |
| Source note | uspto-grants-2008_04 |