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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 56503Erstellt: 24. Oktober 2026

Bromoform → 2-(4-Isopropoxyphenyl)-2-methoxyacetic acid

https://huagongshe.com/de/reaction/56503

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromoformHCID 5558—
EduktPotassium HydroxideHCID 14797—
Edukt1,4-DioxaneHCID 31275—
Edukt4-IsopropoxybenzaldehydeHCID 250077—
EduktPotassium hydroxide methanolHCID 23689386—
LösungsmittelMethanolHCID 887—
Produkt2-(4-Isopropoxyphenyl)-2-methoxyacetic acidHCID 58432042—

Reaktionsschritte

An oven-dried flask was charged with 4-isopropoxybenzaldehyde (4.9 g, 29.9 mmol), anhydrous methanol (30 mL) and anhydrous dioxane (30 mL) then fitted with an addition funnel. The addition funnel was charged with a solution of KOH (8.4 g, 149.5 mmol) in anhydrous methanol (30 mL) and an aliquot (˜2 mL) was added to the reaction mixture. Bromoform (3.4 mL, 38.8 mmol) was added to the reaction mixture then the remaining KOH/MeOH solution was added dropwise over 10 minutes. After stirring for 18 hours, the mixture was concentrated in vacuo. The residue was diluted with water and the pH was adjusted to ˜2 using concentrated HCl then extracted with EtOAc. The combined organics were dried over Na2SO4 and filtered. Concentration of the filtrate in vacuo gave 2-(4-isopropoxyphenyl)-2-methoxyacetic acid as a light yellow solid (6.8 g) which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434707B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-e9c5eccb47884e1e8730c24ca8b655c2
Quellennotizuspto-grants-2016_09