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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38631Erstellt: 23. Oktober 2026

Acetovanillone → 2',3'-Dihydroxyacetophenone

https://huagongshe.com/de/reaction/38631

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetovanilloneHCID 2214—
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
LösungsmittelAcetonitrileHCID 6342—
Produkt2',3'-DihydroxyacetophenoneHCID 642911070,3%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a solution of acetovanillone (33) (4.70 g, 28.3 mmol) in MeCN (60 mL) was added K2CO3 (8.05 g, 58.3 mmol) and KI (0.20 g, 1.2 mmol). The mixture was stirred under N2 atmosphere and benzyl bromide (34) (4.0 mL, 34 mmol) was added dropwise. The reaction mixture was reflux for 24 h and then cooled to 25° C., then resulting precipitate was filtered off. The filtrate was evaporated and purified by column chromatography (SiO2, n-hexane: CH2Cl2=1:2) to give 30. White solid; yield: 70.3%; mp 87-88° C.; 1H-NMR (CDCl3. 200 MHz): δ 2.51 (s, 3H), 3.91 (s, 3H), 5.20 (s, 2H), 6.86 (d, J=8.2 Hz, 1H), 7.21-7.55 (m, 7H); 13C-NMR (CDCl3, 50 MHz): δ 26.19, 56.05, 70.79, 110.53, 112.13, 123.07, 127.18, 128.10, 128.68, 130.72, 136.28, 149.49, 152.41, 196.80; Anal. calcd for C16H16O3: C, 74.98; H, 6.29. Found: C, 75.02; H, 6.25.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524740B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-904a19f9ad764a429ae73edd9fd181c0
Quellennotizuspto-grants-2013_09