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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257348Erstellt: 24. Oktober 2026

M-Cresol → 2-Hydroxy-4-methylbenzaldehyde

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktM-CresolHCID 342—
EduktFormaldehydeHCID 712—
EduktHexamethylphosphoramideHCID 12679—
EduktHCID 178418443HCID 178418443—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Hydroxy-4-methylbenzaldehydeHCID 6120046,3%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05262390
Quelldatensatzuspto-grants-1993_11
ORD IDord-b3aa8d4c6b70478ba1e3adf0a5cf9b5b
Quellennotizuspto-grants-1993_11