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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353308생성일: 2026년 10월 25일

Acetic Acid → HCID 68616271, 화합물

https://huagongshe.com/reaction/353308

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참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물p-Toluenesulfonic acidHCID 6101—
반응물Ethyl ethoxyacetateHCID 69955—
반응물4-(Benzyloxy)-3-methylbenzaldehydeHCID 20298646—
반응물Potassium tert-butoxideHCID 23665647—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물HCID 68616271HCID 6861627125%

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온도-20 °C

반응 단계

4-(Benzyloxy)-3-methylbenzaldehyde (2.36 g; 10.2 mmole) and ethyl ethoxyacetate (1.62 g; 12.3 mmole) were dissolved in dry THF (10 ml) and cooled to −20° C. Potassium tert-butoxide (1.38 g; 12.3 mmole) dissolved in dry tetrahydrofuran (1 ml) was slowly added and the reaction was stirred over night at −20° C. The reaction was quenched with acetic acid (0.80 g; 13.3 mmole). The crude product was isolated, redissolved in toluene and refluxed overnight with p-toluenesulfonic acid (0.18 g; 1.0 mmole) in a Dean-Stark apparatus to separate the water. The solution was cooled, washed with sodium hydrogen carbonate, dried with magnesium sulfate and evaporated. Purification of the crude product with preparative HPLC (Kromasil C8, 10 μm, 50×500 mm) using acetronitrile (50-100%) in ammonium acetate buffer (pH 7) as mobile phase gave 0.86 g (25% yield) of ethyl (2Z)-3-[4-(benzyloxy)-3-methylphenyl]-2-ethoxyacrylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06750252B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-df3f7efd7d2142ceac1d36c76767c65b
출처 메모uspto-grants-2004_06