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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489388Generated: October 30, 2026

Dimethylformamide → 2-[(4-chlorobenzyl)oxy]benzaldehyde

https://huagongshe.com/reaction/1489388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSalicylaldehydeHCID 6998—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantPotassium CarbonateHCID 11430—
SolventDiethyl EtherHCID 3283—
Product2-[(4-chlorobenzyl)oxy]benzaldehydeHCID 693299—

Reaction Steps

Potassium carbonate (33.17 g) and DMF (180 ml) were added to salicylaldehyde (24.42 g), and the mixture was stirred at room temperature for 10 minutes. Then a mixture of 4-chlorobenzyl chloride (33.82 g) and DMF (20 ml) was added at room temperature over 15 minutes, and the mixture was stirred at 60° C. for 3 hours. After completion of the reaction, ether (500 ml) was added, and the mixture was washed with water (400 ml) three times, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give crude 2-(4-chlorobenzyloxy)benzaldehyde. The ethanol (200 ml) and hydroxylamine hydrochloride (27.80 g) was added to the crude product, and the mixture was stirred at 80° C. overnight. After completion of the reaction, water (400 ml) was added, and the mixture was extracted with methylene chloride (200 ml) three times, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting crude product was recrystallized from ethyl acetate/n-hexane to give 2-(4-chlorobenzyloxy)benzaldehyde oxime (32.06 g) as colorless crystals. mp. 122.5°-123.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677465
Source datasetuspto-grants-1997_10
ORD IDord-ea2cf299aa4c4fed8fc8942e7d2686d9
Source noteuspto-grants-1997_10