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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257348생성일: 2026년 10월 24일

M-Cresol → 2-Hydroxy-4-methylbenzaldehyde

https://huagongshe.com/ko/reaction/257348

반응식

참여 물질

역할이름HCID투입량
반응물M-CresolHCID 342—
반응물FormaldehydeHCID 712—
반응물HexamethylphosphoramideHCID 12679—
반응물HCID 178418443HCID 178418443—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2-Hydroxy-4-methylbenzaldehydeHCID 6120046.3%

반응 단계

A 1M solution of ethylmagnesium bromide in tetrahydrofuran (100 ml) was cooled to 15° C., and a solution of 10.81 g (0.100 mole) of m-cresol was added during a 45 minute period while the temperature was held at 15° C. Upon completion of the addition, the mixture was stirred at room temperature for 30 minutes, and then a mixture of 7.5 g (0.25 mole) of paraformaldehyde and 17.92 g (0.100 mole) of hexamethylphosphoramide in 200 mL of toluene was added in one portion. The resulting solution was heated at 80° C. for approximately seventeen hours, after which the solvent was evaporated under reduced pressure, leaving a yellow residue. This residue was dissolved in diethyl ether, and this solution was extracted with 50 mL of hydrochloric acid and 100 mL of water. The organic phase was separated, washed with water, and dried over anhydrous magnesium sulfate. After filtration the solution was evaporated under reduced pressure, leaving an orange solid as a residue. This solid was placed on a silica gel column and eluted with methylene chloride/petroleum ether (50/50). Evaporation of the solvents yielded 6.30 g of 4-methylsalicylaldehyde as a yellow solid, m.p. 51°-53° C. The NMR and IR spectra were consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05262390
출처 데이터셋uspto-grants-1993_11
ORD IDord-b3aa8d4c6b70478ba1e3adf0a5cf9b5b
출처 메모uspto-grants-1993_11