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HRID 257348作成日:2026年10月26日

M-Cresol → 2-Hydroxy-4-methylbenzaldehyde

https://huagongshe.com/reaction/257348

反応式

関与物質

役割名称HCID仕込み量
反応物M-CresolHCID 342—
反応物FormaldehydeHCID 712—
反応物HexamethylphosphoramideHCID 12679—
反応物HCID 178418443HCID 178418443—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物2-Hydroxy-4-methylbenzaldehydeHCID 6120046.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05262390
出典データセットuspto-grants-1993_11
ORD IDord-b3aa8d4c6b70478ba1e3adf0a5cf9b5b
出典メモuspto-grants-1993_11