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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1662144Erstellt: 27. Oktober 2026

3-Isopropylsalicylic acid → 1-[2-Hydroxy-3-(propan-2-yl)phenyl]ethan-1-one

https://huagongshe.com/reaction/1662144

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Isopropylsalicylic acidHCID 201887—
EduktHCID 178418348HCID 178418348—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-[2-Hydroxy-3-(propan-2-yl)phenyl]ethan-1-oneHCID 66683681—

Reaktionsbedingungen

Temperatur-75 °C

Reaktionsschritte

2-Hydroxy-3-isopropylbenzoic acid (Aldrich, 4.0 g, 22.2 mmol) was dissolved in tetrahydrofuran (20 mL), chilled to −75° C., and methyllithium (1.6M in diethyl ether, 42 mL, 66.6 mmol) was added. The mixture stirred overnight at ambient temperature. The mixture was quenched with methanol (50 mL), concentrate under reduced pressure, and ethyl acetate (200 mL) was added. The mixture was washed with 1N hydrochloric acid (200 mL), water (200 mL), and brine and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrate under reduced pressure. The residue was chromatographed on silica gel eluting with 0-to-30% ethyl acetate in hexane to afford the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 1.23 (d, 6H), 2.64 (s, 3H), 3.39 (m, 1H), 6.87 (t, 1H), 7.41 (dd, 1H), 7.59 (dd, 1H), 12.69 (s, 1H). MS (DCI) m/z 179.07 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08030504B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-c219d5993e1f45999b433bf4c6766c47
Quellennotizuspto-grants-2011_10