HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
p-Toluenesulfonic acid → 5-Hexadecene, 16,16-diethoxy-, (5Z)-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 2-Heptanone | HCID 8051 | — |
| Edukt | Neral | HCID 643779 | — |
| Edukt | 11-Hexadecenal, (11Z)- | HCID 5364495 | — |
| Katalysator | Ammonium Chloride | HCID 25517 | — |
| Produkt | 5-Hexadecene, 16,16-diethoxy-, (5Z)- | HCID 6438017 | 61,5% |
Reaktionsschritte
The diethyl acetal or ketal is prepared by the above general procedure from (Z)-11-hexadecenal, (E)-and (Z)-citral in admixture and heptan-2-one using NH4Cl as catalyst in the first two cases and TsOH in the last. (Z)-1,1-Diethoxyhexadec-11-ene is obtained in 61.5% yield and has a b.p. 118°-120°C./0.05 mm, nD20 1.4475; (E)-and (Z)-1,1-diethoxy-3,7-dimethoxyocta-2,6-diene in admixture are obtained in 83.6% yield and have b.p. 68°-70°C./0.2 mm, nD20 1.4511; 2,2-diethoxyheptane is obtained in 71% yield and has b.p. 88°-92°C./18 mm.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04657926 |
| Quelldatensatz | uspto-grants-1987_04 |
| ORD ID | ord-b9e4481c70e942cfbd66ddfd7aba01d9 |
| Quellennotiz | uspto-grants-1987_04 |