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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 543340Erstellt: 24. Oktober 2026

Vanillin → Ethyl 3-methyl-4-(4-formyl-2-methoxyphenoxy)-2-butenoate

https://huagongshe.com/de/reaction/543340

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVanillinHCID 1183—
EduktSodium HydroxideHCID 14798—
EduktSodium hydrideHCID 24758—
EduktEthyl-4-bromo-3-methyl-but-2-enoate (E/Z; 55/45)HCID 53411540—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl 3-methyl-4-(4-formyl-2-methoxyphenoxy)-2-butenoateHCID 54099897—

Reaktionsschritte

Vanillin (3.43 g, 22.5 mmol) in 10 ml of DMF is added portionwise, at 0°, to sodium hydride (21.5 g, 23.6 mmol) in ml of DMF. The mixture is stirred for 10 min. and then ethyl 4-bromo-3-methyl-2-butenoate (4.87 g, 23.5 mmol) in 3 ml of DMF is added. After 3 hours, the reaction mixture is poured into ether and 5% sodium hydroxide solution. The aqueous layer is extracted with ether, and the organic layers are combined and washed with 5% sodium hydroxide, with water and with brine and dried. Solvent is removed in vacuo and the crude product is chromatographed to give ethyl 3-methyl-4-(4-formyl-2-methoxyphenoxy)-2-butenoate. To isopropyltriphenylphosphonium iodide (2.26 g, 5.23 mmol) in 15 ml of tetrahydrofuran (THF) is added n-butyllithium (1.6 M; 3.10 ml, 5.0 mmol) at -5°. The mixture is cooled to -60°, and ethyl 3-methyl-4-(4-formyl-2-methoxyphenoxy)-2-butenoate (0.70 g, 2.51 mmol) in 10 ml of THF is added. After 45 min. the reaction mixture is poured into ether and water, and the aqueous phase is extracted with ether. The combined ether layers are washed with water and with brine and dried. Solvent is removed in vacuo, and the crude product is triturated with hexane and the hexane-soluble fraction is purified by prep. TLC to give ethyl 3-methyl-4-[2-methoxy-4-(2-methyl-1-propenyl)phenoxy]-2-butenoate, MS m/e 304 (M+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04661617
Quelldatensatzuspto-grants-1987_04
ORD IDord-f89dbe30299a48088a96a06045b70f3b
Quellennotizuspto-grants-1987_04