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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 343281생성일: 2026년 10월 24일

Formaldehyde → 4-Ethyl-2-hydroxybenzaldehyde

https://huagongshe.com/ko/reaction/343281

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물3-EthylphenolHCID 12101—
반응물HexamethylphosphoramideHCID 12679—
반응물HCID 178418443HCID 178418443—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물4-Ethyl-2-hydroxybenzaldehydeHCID 1023601769.1%

반응 단계

A stirred solution of 200 mL (0.20 mole) of 1.0M of ethylmagnesium bromide (in tetrahydrofuran) in 100 mL of tetrahydrofuran was cooled in an ice-bath and 25.0 grams (0.21 mole) of 3-ethylphenol was added dropwise. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature where it stirred for 30 minutes. After this time, 15.4 grams (0.51 mole) of paraformaldehyde, 36.7 grams (0.21 mole) of hexamethylphosphoramide, and 350 mL of toluene were added. Upon completion of addition, the reaction mixture was heated to 80° C. where it stirred for about 18 hours. The reaction mixture was then cooled and concentrated under reduced pressure to a residue. The residue was taken up in diethyl ether and 200 mL of an aqueous 10% hydrochloric acid solution was added. The aqueous layer was separated and extracted with diethyl ether. The extract was combined with the organic layer, and the combination was washed with water. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduce pressure to a residue. The residue was subjected to column chromatography on silica gel, using 1:1 hexane and methylene chloride as the eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding 21.8 grams of 5-ethyl-2-formylphenol. The NMR spectrum was consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05861359
출처 데이터셋uspto-grants-1999_01
ORD IDord-b707ed1977ce42ceb5dcd42e9d14fa47
출처 메모uspto-grants-1999_01