HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1283356Erstellt: 26. Oktober 2026
3,7-Dimethylocta-2,6-Dienal → 6,10-Dimethyl-4-hydroxy-2,5,9-undecatriene
https://huagongshe.com/reaction/1283356
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3,7-Dimethylocta-2,6-Dienal | HCID 8843 | — |
| Edukt | 1-Bromo-1-propene | HCID 11533 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 6,10-Dimethyl-4-hydroxy-2,5,9-undecatriene | HCID 54549445 | — |
Reaktionsschritte
12 g. of magnesium turnings were suspended under nitrogen in 250 ml. of dry tetrahydrofuran. Between 60 and 65°, 60 g. of 1-bromopropene dissolved in 50 ml of tetrahydrofuran were added dropwise. During the addition, to prevent escaping of 1-bromopropene, the reflux condenser fitted on the reaction flask was cooled to -40°/-50°. When all Mg had reacted, the mixture was cooled to 20° and 76 g. of citral was added dropwise with cooling. After standing overnight, the mixture was poured into 1.5 liter of concentrated aqueous NH4Cl at 0°. The mixture was extracted 3 times with ether and the combined ether extracts treated as usual. After distillation, 6,10-dimethyl-4-hydroxy-2,5,9-undecatriene, b.p. 70°/0.1 Torr was obtained as a liquid with following constants: nD20 = 1.4950; d420 = 0.9145.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03975310 |
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| Quelldatensatz | uspto-grants-1976_08 |
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| ORD ID | ord-b662e75be2da4e94bebaf83ee0707516 |
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| Quellennotiz | uspto-grants-1976_08 |
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