Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488393Generated: October 26, 2026

Potassium Carbonate → Methyl 2-(5-chloro-2-formylphenoxy)propionate

https://huagongshe.com/reaction/1488393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-bromopropionateHCID 95576—
Reactant4-Chloro-2-hydroxybenzaldehydeHCID 520101—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(5-chloro-2-formylphenoxy)propionateHCID 5380006018.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 22.0 g (0.141 mole) of 4-chlorosalicylaldehyde, 30 g (0.22 mole) of anhydrous potassium carbonate, and 30.0 g (0.184 mole) of methyl 2-bromopropionate in 120 mL of N,N-dimethylformamide was heated at 80° C. for approximately 17 hours. At the end of that period, the reaction mixture was poured over ice and extracted successively with diethyl ether and ethyl acetate. The combined extracts were washed with water, dried over anhydrous magnesium sulfate, and filtered. The solvents were then evaporated under reduced pressure, leaving a residue weighing 20 g. This residue was purified by placing it on a silica gel column and eluting with diethyl ether/petroleum ether (25/75). After the product-containing fractions were combined and the solvents evaporated under reduced pressure, 6.23 g of methyl 2-(5-chloro-2-formylphenoxy)propionate was isolated as a yellow liquid. Similarly, other fractions were combined and evaporated, yielding 1.69 g of methyl 2-(3-chloro-2-formylphenoxy)propionate as a yellow liquid. The NMR spectra of both compounds were consistent with proposed structure of each. This reaction was repeated several times.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674810
Source datasetuspto-grants-1997_10
ORD IDord-ab57be8b7c424e8a878abc5a165edee9
Source noteuspto-grants-1997_10