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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367061Generated: October 30, 2026

Potassium Carbonate → 3-(Cyclopropylmethoxy)-4-(difluoromethoxy)benzaldehyde

https://huagongshe.com/reaction/1367061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Difluoromethoxy)-3-hydroxybenzaldehydeHCID 2758295—
Reactant(2-Bromoethyl)cyclopropaneHCID 22636989—
SolventDimethylformamideHCID 6228—
Product3-(Cyclopropylmethoxy)-4-(difluoromethoxy)benzaldehydeHCID 18973698100%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a mixture of 4-difluoromethoxy-3-hydroxy-benzaldehyde (5.0 g, 27 mmol) and potassium carbonate (5.5 g, 40 mmol) in dimethylformamide (30 ml) under inert atmosphere at 60° C. was added bromoethylcyclopropane (5 g, 37 mmol). The mixture was stirred and heated at 65° C. After 1.5 hour, the mixture was allowed to cool and was filtered. The filtrate was concentrated under reduced pressure. The mixture was extracted with ethyl acetate (2×25 ml) and water (25 ml). The organic layer was washed with water (25 ml), brine (25 ml) and dried over magnesium sulfate. The solvent was removed in vacuo to give 3-cyclopropylmethoxy-4-difluoromethoxy-benzaldehyde as an oil (6.4 g, 100%). 1HNMR (CDCl3): δ 0.38-0.44 (m, 2H), 0.62-0.75 (m, 2H), 1.15-1.36 (m, 1H), 3.98 (d, J=4.5 Hz, 2H), 6.78 (t, JH-F=75 Hz, 1H), 7.30-7.50 (m, 3H), 9.96 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893102B2
Source datasetuspto-grants-2011_02
ORD IDord-e6c178f096b94e04a74a3046ffd024e4
Source noteuspto-grants-2011_02