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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359162Generated: October 31, 2026

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

https://huagongshe.com/reaction/2359162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantPotassium HydroxideHCID 14797—
Reactant1,4-DioxaneHCID 31275—
Reactant4-IsopropoxybenzaldehydeHCID 250077—
ReactantPotassium hydroxide methanolHCID 23689386—
SolventMethanolHCID 887—
Product2-(4-Isopropoxyphenyl)-2-methoxyacetic acidHCID 58432042—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685975B2
Source datasetuspto-grants-2014_04
ORD IDord-dd44a53846e04641b8ee54bead7d800c
Source noteuspto-grants-2014_04