HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoethene → HCID 14261103, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoethene | HCID 11641 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Cyclohexylacetaldehyde | HCID 316627 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14261103 | HCID 14261103 | — |
Reaction Steps
A solution of 60 g (0.47 mol) of cyclohexylacetaldehyde in 400 ml of abs. THF is added dropwise at -20° to a solution of vinylmagnesium bromide in abs. THF, prepared from 13.8 g (0.57 mol) of magnesium and 66.3 g (0.62 mol) of vinyl bromide in 500 ml of abs. THF. When the addition is complete, the whole is stirred for 30 minutes at -20° and then hydrolysed with 900 ml of saturated ammonium chloride solution. After diluting with 250 ml of H2O, the reaction mixture is extracted three times with 1 liter of ether each time, washed three times with 500 ml of brine each time, dried with MgSO4 and then concentrated by evaporation in a rotary evaporator. The residue is distilled at 50°/0.1 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05010189 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-207ae8b811c04f419c97e9c4c0d324c1 |
| Source note | uspto-grants-1991_04 |