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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798571Generated: October 30, 2026

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

https://huagongshe.com/reaction/1798571

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 numberUS08343970B2
Source datasetuspto-grants-2013_01
ORD IDord-f81d3c8448934979ad09d0f4db530a5a
Source noteuspto-grants-2013_01