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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384115Generated: October 29, 2026

Citric Acid → (2-Isopropoxyphenyl)methanol

https://huagongshe.com/reaction/384115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantHydrochloric AcidHCID 313—
ReactantSalicylaldehydeHCID 6998—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Solvent2-BromopropaneHCID 6358—
Product(2-Isopropoxyphenyl)methanolHCID 12071269—

Reaction Steps

To a solution of 2-hydroxybenzaldehyde (0.5 ml) in dimethylformamide (5 ml), 1.35 ml of 2-bromopropane and 1.98 g of potassium carbonate were added, and the reaction solution was stirred overnight at room temperature. To the reaction solution was added 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to afford a crude product as a yellow oil. To a solution of the crude product in methanol (5 ml), 362 mg of sodium borohydride was added under ice-cooling, and the reaction solution was stirred at room temperature for 30 minutes. To the reaction solution was added 10% aqueous citric acid, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (98:2-50:50)) to afford the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367708B2
Source datasetuspto-grants-2013_02
ORD IDord-6bf5fc07978646e39906b94f6909d3bd
Source noteuspto-grants-2013_02