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HRID 27849Erstellt: 23. Oktober 2026

1,2-Epoxybutane → 3,7-Dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester

https://huagongshe.com/de/reaction/27849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-EpoxybutaneHCID 7834—
EduktButyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoateHCID 53845956—
Edukt3-Chloro-2,4,6-trimethyl-benzyl-triphenylphosphonium chlorideHCID 86735897—
Produkt3,7-Dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl esterHCID 54292054—

Reaktionsschritte

16 g of 3-chloro-2,4,6-trimethyl-benzyl-triphenylphosphonium chloride and 10 g of 7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid butyl ester are heated to boiling with stirring after the addition of 40 g of 1,2-butylene oxide. The 1,2-butylene oxide is slowly distilled off. The reaction mixture is stirred for 30 minutes at 80°-82° C., then cooled and thoroughly extracted with hexane. The hexane extract is shaken out 5 times with 50 ml of methanol/water 70:30 parts by volume each time, then dried over sodium sulphate and evaporated under reduced pressure to produce 9-(3-chloro-2,4,6-trimethyl-phenyl), 3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester as a residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04224244
Quelldatensatzuspto-grants-1980_09
ORD IDord-5a0510b3ae024dbeafefae45eb02d3e0
Quellennotizuspto-grants-1980_09