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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2387021Erstellt: 24. Oktober 2026

3-Ethylphenol → 4-Ethyl-2-hydroxybenzaldehyde

https://huagongshe.com/de/reaction/2387021

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-EthylphenolHCID 12101—
EduktMethane, dichloromethoxy-HCID 21004—
KatalysatorTitanium TetrachlorideHCID 24193—
Produkt4-Ethyl-2-hydroxybenzaldehydeHCID 1023601765,3%

Reaktionsschritte

Titanium(IV) chloride (100 mL, 100 mmol, 1M in CH2Cl2) followed by dichloromethyl methyl ether (7.47 mL, 82.5 mmol) was added to a cooled 0° C. solution of 3-ethylphenol (6.11 g, 50 mmol). The reaction mixture was stirred for 45 mins. The mixture was poured into ice and extracted with EtOAc. The organic layers were washed with brine, dried over Na2SO4 and concentrated to a bright pink oil. Purification by flash column chromatography (0% to 10% EtOAc in hexanes) gave 4-ethyl-2-hydroxy-benzaldehyde (4.9 g, 65%) followed by 2-ethyl-4-hydroxy-benzaldehyde (1.32 g, 18%). A: 1H NMR (400 MHz, CDCl3): δ 1.25 (t, J=7.6 Hz, 3 H), 2.67 (d, J=7.6 Hz, 2 H), 6.82 (s, 1 H), 6.85 (d, J=8.0 Hz, 1 H), 7.46 (t, J=8.0 Hz, 1 H), 9.83 (s, 1 H), 11.05 (s, 1 H). B: 1H NMR (400 MHz, CDCl3): δ 1.27 (t, J=7.6 Hz, 3 H), 3.03 (d, J=7.6 Hz, 2 H), 6.68 (s, 1 H), 6.78 (s, 1 H), 6.82 (d, J=8.3 Hz, 1 H), 7.77 (t, J=8.3 Hz, 1 H), 10.10 (s, 1 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08268835B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-521b495bb2af4e898272e25ab57e6c39
Quellennotizuspto-grants-2012_09