HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrolein → HCID 20144474, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrolein | HCID 7847 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Isopropenylacetylene | HCID 62323 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 20144474 | HCID 20144474 | — |
Reaction Steps
10 g Isopropenylacetylene are taken up in abs. tetrahydrofuran and under an inert gas 94.5 ml of 1.6M solution of n-butyllithium in hexane added dropwise at -20°. The mixture is then cooled to -78° and 8.5 g of acrolein added dropwise. The reaction mixture is warmed to room temperature, poured into saturated aqueous NH4Cl and repeatedly extracted with ether. The organic phase is washed, dried and concentrated in vacuum. An oil is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04737516 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-0a33d5a5bccb415e8fff42413fad8b60 |
| Source note | uspto-grants-1988_04 |