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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701141Generated: November 1, 2026

4-Hydroxybenzaldehyde → p-(Difluoromethoxy)benzaldehyde

https://huagongshe.com/reaction/1701141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantChlorodifluoromethaneHCID 6372—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Productp-(Difluoromethoxy)benzaldehydeHCID 273698659.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

Sodium hydroxide (48 g; 1.2 mole) is added to a stirred suspension of p-hydroxybenzaldehyde (48.9 g; 0.4 mole) in dioxane (142 ml) and water (87 ml). The mixture is heated to 70° C. and chlorodifluoromethane (33 g) added slowly. When this addition is completed, 50% sodium hydroxide solution (32 ml) is added to the reaction mixture, followed by the slow addition of chlorodifluoromethane (33 g). This recharging is repeated three times, and a total of 96 g (2.4 mole) of sodium hydroxide and 133 g (1.54 mole) of (1.54 mole) of chlorodifluoromethane is used in the reaction. The reaction mixture is cooled down, diluted with water (1500 ml) and extracted with ether several times. The ether layers are combined, washed with 10% sodium hydroxide and then dried over magnesium sulfate. Concentration of the ethereal solution yields 39 g (57%) of a yellow oil. This oil is purified by chromatography on a silica gel column using a mixture of hexane:methylene chloride (1:3), to afford 27 g (39%) of title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04191768
Source datasetuspto-grants-1980_03
ORD IDord-0e297ddeaf134399ae50ae6fb1301aef
Source noteuspto-grants-1980_03