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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257355Generated: October 25, 2026

Formaldehyde → 4-Chloro-2-hydroxybenzaldehyde

https://huagongshe.com/reaction/257355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant3-ChlorophenolHCID 7933—
ReactantTetrahydrofuranHCID 8028—
ReactantHexamethylphosphoramideHCID 12679—
ReactantHCID 178418443HCID 178418443—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product4-Chloro-2-hydroxybenzaldehydeHCID 52010173.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A 2M solution of ethylmagnesium bromide in tetrahydrofuran (50 ml, 0.10 mole) was placed in a flask, and a solution of 12.85 g (0.10 mole) of 3-chlorophenol in 50 mL of diethyl ether was added slowly with stirring. The addition required two hours, after which the solvents were removed by evaporation under reduced pressure. Toluene (200 ml), 7.50 g (0.25 mole) of paraformaldehyde, and 17.92 g (0.10 mole) of hexamethylphosphoramide were added to the residue, and this mixture was heated at 80° C. for approximately 16 hours. The solvent was evaporated under reduced pressure, leaving a residue. This residue was washed successively with 50 mL of hydrochloric acid and 300 mL of water. Vacuum distillation of the washed residue yielded 11.50 g of 4-chlorosalicylaldehyde, b.p. 112° C. at 9 mm of Hg. This reaction was repeated several times.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262390
Source datasetuspto-grants-1993_11
ORD IDord-e8df0bebc4294be48db9951d1906c2d9
Source noteuspto-grants-1993_11