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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 377116생성일: 2026년 10월 26일

4-Hydroxybenzaldehyde → Benzaldehyde, 4-[2-(5-ethyl-2-pyridinyl)ethoxy]-

https://huagongshe.com/reaction/377116

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참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Sodium HydroxideHCID 14798—
반응물5-Ethyl-2-pyridineethanolHCID 78894—
촉매Benzyltributylammonium chlorideHCID 159952—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
생성물Benzaldehyde, 4-[2-(5-ethyl-2-pyridinyl)ethoxy]-HCID 9881522—

반응 조건

온도22 °C

반응 단계

To a mixed solution of 5-ethyl-2-pyridine ethanol (6.0 kg), benzyltributylammonium chloride (6.2 kg of 50% aqueous solution), 1,2-dichloroethane (30 l) and p-toluenesulfonylchloride (9.2 kg) was added dropwise 8N aqueous solution (10 l) of sodium hydroxide at 25° C. After the solution was stirred at 22±3° C. for 4 hours, p-hydroxybenzaldehyde (5.9 kg) and 3N solution (16 l) of sodium hydroxide, were added, and the mixed solution was stirred at 57±3° C. for 15 hours. After the solution was cooled, water (70 l) was added. The aqueous layer was separated and subjected to extraction with 1,2-dichloroethane (20 l). The organic layers were combined and the combined layer was washed three times with 0.1N aqueous solution of sodium hydroxide and three times with water (30 l). The organic layer was concentrated at not higher than 45° C. under a reduced pressure, whereby 4-[2-(5-ethyl-2-pyridyl)ethoxy]benzaldehyde was obtained as an oil. Quantitative analysis by HPLC (high performance liquid chromatography) showed that 5.98 kg (59.0%) of 4-[2-(5-ethyl-2-pyridyl)ethoxy]benzaldehyde was included in this crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE036575
출처 데이터셋uspto-grants-2000_02
ORD IDord-828def491caf4792a7e5dca6256d166e
출처 메모uspto-grants-2000_02