HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 6,6-Dimethylhepta-2,4-dienal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Buten-3-yne, 1-methoxy- | HCID 97983 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 178418586 | HCID 178418586 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6,6-Dimethylhepta-2,4-dienal | HCID 54533025 | — |
Reaction Steps
Freshly distilled 4-methoxy-but-3-en-1-yne is added dropwise under cooling to a solution of t-butyl-magnesium bromide in absolute tetrahydrofuran and the mixture stirred for 45 minutes at room temperature. The reaction mixture is first mixed with 13.6 g of ethanol, then, under cooling and inert gas atmosphere, reacted with 5.9 g of LiAlH4 and stirred overnight at room temperature. It is then mixed with saturated aqueous NH4Cl under cooling, acidified with H2SO4 and extracted with ether. The pure product is obtained by vacuum distillation b.p. (bulb tube) 50°/0.26 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04382951 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-c5a68c4760de42b388f6b92b21bc938b |
| Source note | uspto-grants-1983_05 |