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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2225502Erstellt: 26. Oktober 2026

Sodium Chloride → Allyl 3-[1-(4-allyloxycarbonyl-4-methylcyclohexyl)methoxy]-4-methoxycinnamate

https://huagongshe.com/reaction/2225502

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
EduktPotassium CarbonateHCID 11430—
Edukt3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acidHCID 92126—
EduktAllyl 4-iodomethyl-methyl-1-cyclohexanecarboxylateHCID 19004693—
EduktAllyl 3-hydroxy-4-methoxycinnamateHCID 54483065—
LösungsmittelDimethylformamideHCID 6228—
ProduktAllyl 3-[1-(4-allyloxycarbonyl-4-methylcyclohexyl)methoxy]-4-methoxycinnamateHCID 5366056547,8%

Reaktionsschritte

5 g of potassium carbonate and 1.1 g of allyl 4-iodomethyl-methyl-1-cyclohexanecarboxylate (Example 46) were added to a solution of 0.8 g of allyl 3-hydroxy-4-methoxycinnamate, derived from 3-hydroxy-4-methoxycinnamic acid by the allyl-esterification thereof, in 50 ml of DMF. The solution was reacted for 18 hours at 100° C. After reaction, 100 ml of an aqueous sodium chloride solution was added to the reaction solution. The solution was extracted three times with 50 ml of ethyl acetate. The organic layer obtained was washed three times with an aqueous sodium chloride solution and was dried over magnesium sulfate. Thereafter, the solvent was removed in vacuo. The oily substance obtained was subjected to column chromatography using 5 g of silica gel. From the fraction eluted with hexane and ethyl acetate=2:1, the solvent was removed in vacuo, yielding 0.7 g of allyl 3-[1-(4-allyloxycarbonyl-4-methylcyclohexyl)methoxy]-4-methoxycinnamate (a compound of the present invention) as a pale yellow oil, which had the following physiochemical properties:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05344845
Quelldatensatzuspto-grants-1994_09
ORD IDord-b72f1d0f28b24e76b206ef87c3772fc8
Quellennotizuspto-grants-1994_09