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HRID 28104Erstellt: 23. Oktober 2026

1,2-Epoxybutane → 9-(2,6-Dichloro-4-methoxy-5-methyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid ethyl ester

https://huagongshe.com/de/reaction/28104

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-EpoxybutaneHCID 7834—
EduktTriphenylphosphineHCID 11776—
Edukt2,6-Dichloro-4-methoxy-3-methyl-benzyl chlorideHCID 23462577—
EduktEthyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoateHCID 54295620—
Edukt(2,6-Dichloro-3-methyl-4-methoxybenzyl) triphenyl phosphonium chlorideHCID 86736665—
LösungsmittelToluene hexaneHCID 21889329—
Produkt9-(2,6-Dichloro-4-methoxy-5-methyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid ethyl esterHCID 127591—

Reaktionsschritte

100 g. of 2,6-dichloro-4-methoxy-5-methyl-benzyl-triphenylphosphonium chloride, prepared from 52 g. of 2,6-dichloro-4-methoxy-3-methyl-benzyl chloride and 57 g. of triphenylphosphine, are treated with 42 g. of 7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid ethyl ester. After the addition of 120 ml. of 1,2-butylene oxide, the resulting mixture is heated to 80°-85° C. for 4 hours while stirring. The mixture is diluted with toluene/hexane (1:1 parts by volume) and exhaustively extracted with methanol/water (60:40 parts by volume). The resulting solution is evaporated under reduced pressure. The oily residue is purified by adsorption on silica gel using toluene for the elution. 9-(2,6-dichloro-4-methoxy-5-methyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid ethyl ester is obtained from the eluate and melts at 100°-101° C. after recrystallization from benzene/hexane (50:50 parts by volume).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04225527
Quelldatensatzuspto-grants-1980_09
ORD IDord-c89e883b75a84e41afb4b1f8004b6ddf
Quellennotizuspto-grants-1980_09