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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249346Generated: November 1, 2026

Salicylaldehyde → HCID 10899688, compound

https://huagongshe.com/reaction/1249346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromocyclohexeneHCID 137057—
SolventAcetoneHCID 180—
ProductHCID 10899688HCID 1089968892.9%

Reaction Steps

In a 10-liter reactor there were introduced 633.4 g (5.19 moles) of salicylaldehyde, 5 liters of acetone and 717.3 g of potassium carbonate, and the mixture was left with stirring at room temperature. After precipitation of the phenate, 836 g (5.19 moles) of 3-bromocyclohexene were rapidly added dropwise, and the mixture was brought to reflux for 21/2 hours. After removal of the inorganic salts by filtration, and evaporation of the solvent, the residue was taken up in ethyl ether, washed with 10% caustic soda and then water, and the ether phase was then dried over Na2SO4. After filtration and elimination of the ether, there were obtained 975 g of 3-(2-formylphenoxy)cyclohexene, which was used directly in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04631277
Source datasetuspto-grants-1986_12
ORD IDord-85daf6bea9884c8197cecc290f059289
Source noteuspto-grants-1986_12