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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 543340생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/543340

반응식

참여 물질

역할이름HCID투입량
반응물VanillinHCID 1183—
반응물Sodium HydroxideHCID 14798—
반응물Sodium hydrideHCID 24758—
반응물Ethyl-4-bromo-3-methyl-but-2-enoate (E/Z; 55/45)HCID 53411540—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물Ethyl 3-methyl-4-(4-formyl-2-methoxyphenoxy)-2-butenoateHCID 54099897—

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04661617
출처 데이터셋uspto-grants-1987_04
ORD IDord-f89dbe30299a48088a96a06045b70f3b
출처 메모uspto-grants-1987_04