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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 903298Erstellt: 26. Oktober 2026

Propyne → beta-Damascenone, (2Z)-

https://huagongshe.com/reaction/903298

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropyneHCID 6335—
Edukt3,7-Dimethylocta-2,6-DienalHCID 8843—
Edukt2,6,6-Trimethyl-1-[1-hydroxy-2-butynyl]-1,3-cyclohexadieneHCID 23338079—
Edukt6,10-Dimethylundeca-2,5,9-trien-4-oneHCID 54158364—
Edukt6,10-Dimethyl-4-hydroxy-2,5,9-undecatrieneHCID 54549445—
Edukt2,6,6-Trimethyl-1-tetrolyl-1,3-cyclohexadieneHCID 70587951—
KatalysatorManganese dioxideHCID 14801—
Produktbeta-Damascenone, (2Z)-HCID 12309006—

Reaktionsschritte

Safranal, prepared according to Compt. rend. 262, 1725 (1966), was reacted with propyne to give 2,6,6-trimethyl-1[-1-hydroxy-2-butynyl]-1,3-cyclohexadiene, following the procedure outlined in Example 18, paragraph (b), for the reaction of citral with propyne. The above carbinol was oxidised with MnO2 to 2,6,6-trimethyl-1-tetrolyl-1,3-cyclohexadiene, following the procedure described in Example 18, paragraph (c), for the oxidation of the dihydro analogue. The above acetylenic ketone was then partially reduced to the title compound following the method described in Example 18, paragraph (a). Cis-2,6,6-trimethyl-1-crotonoyl-1,3-cyclohexadiene gave the following NMR data (CCl4): 1.06 (6 H, s), 1.69 (3 H, s), 2.09 (2 H, d, J=2.3 cps), 2.14 (3 H, d, J=5.5 cps), 5.81 (2 H, t+s, J=2.3 cps), 6.2 (2 H, complex band) ppm (δ).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04226892
Quelldatensatzuspto-grants-1980_10
ORD IDord-f66eca6e31c14bd4a34efc6fe40fc400
Quellennotizuspto-grants-1980_10