HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 363827Erstellt: 26. Oktober 2026
Isopropanol → 2-Buten-1-ol, 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-
https://huagongshe.com/reaction/363827
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isopropanol | HCID 3776 | — |
| Edukt | Trichloroacetic Acid | HCID 6421 | — |
| Edukt | 2-Methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enal | HCID 3017557 | — |
| Edukt | Aluminum tri-iso-propoxide | HCID 16685055 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-Buten-1-ol, 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)- | HCID 119897 | 81% |
Reaktionsschritte
3.07 g (15 mmol) of Al(O-i-Pr)3 and 30 ml of toluene were fed into a 100 ml four-necked round bottom flask under atmosphere of nitrogen, and stirred at room temperature, and then 28.8 g (150 mmol) of 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-al, then 0.25 g (1.5 mmol) of trichloroacetic acid, and further 18.0 g (300 mmol) of isopropyl alcohol were added while stirring at room temperature. Reaction was conducted while fraction containing acetone generated at the solution temperature of 80° to 92° C. was distilled off. After 6 hours, the reaction solution was analyzed by GLC, 81% of 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol was obtained (corresponding to 90% selectivity for conversion of the aldehyde as the starting material).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05874649 |
|---|
| Quelldatensatz | uspto-grants-1999_02 |
|---|
| ORD ID | ord-3c69ea5d177245898c506b4aba8756cd |
|---|
| Quellennotiz | uspto-grants-1999_02 |
|---|