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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1269154Erstellt: 25. Oktober 2026

Formic Acid → 4-Methyl-alpha-(4-methylphenyl)benzeneacetic acid

https://huagongshe.com/reaction/1269154

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormic AcidHCID 284—
EduktSulfuric AcidHCID 1118—
EduktPotassium HydroxideHCID 14797—
Edukt4,4'-DimethylbenzhydrolHCID 279356—
LösungsmittelWaterHCID 962—
Produkt4-Methyl-alpha-(4-methylphenyl)benzeneacetic acidHCID 3031426%

Reaktionsbedingungen

Temperatur15 °C

Reaktionsschritte

To a 250 mL RB-flask was added 4,4′-dimethylbenzhydrol (1.06 g, 5.00 mmol) and 97% sulfuric acid (44.0 mL). The mixture was cooled to 15° C. by an ice/water bath and formic acid (12.0 mL) was added dropwise via an addition funnel over 0.5 h. The resulting foaming solution was stirred at 15° C. for 2 h. Water (300 mL) was added and the pH was adjusted to 3 with potassium hydroxide pellets and 10% KOH solution. The aqueous solution was extracted with ethyl acetate (3×100 mL) and the combined organic extracts were washed with brine (100 mL) and dried over sodium sulfate, filtered and concentrated in vacuo to give the desired product (0.281 g, 26%) as a pale yellow solid, which was used in the subsequent step without further purification: 1H NMR (400 MHz, CD3OD) δ 7.28–6.99 (m, 8H), 6.96 (br s, 1H), 4.94 (s, 1H), 2.29 (s, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07199135B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-9ab7628de85b441d872d7c397faf11a9
Quellennotizuspto-grants-2007_04