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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268734Generated: November 3, 2026

4-Hydroxybenzaldehyde → 4-[(2,6-dichlorobenzyl)oxy]benzaldehyde

https://huagongshe.com/reaction/2268734

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
SolventDimethylformamideHCID 6228—
Product4-[(2,6-dichlorobenzyl)oxy]benzaldehydeHCID 735466—

Reaction Steps

A suspension of 4-hydroxybenzaldehyde (19.2 g, 157.5 mmol), 2,6-dichlorobenzylbromide (36 g, 150 mmol) and potassium carbonate (22.77 g, 165 mmol) in DMF (150 ml) was stirred at room temperature overnight. The mixture was filtered and the filtrate evaporated under reduced pressure. The residue was dissolved in ether (500 ml), and washed with aqueous NaOH (5%, 100 ml), water (100 ml) and brine (100 ml), dried (Na2SO4) and evaporated under reduced pressure. The orange crystalline solid obtained was recrystallised from diisopropylether to give the title compound as slightly orange needles (35.8 g, 85%), m.p. 70-71°. δH (CDCl3) 9.91 (1H, s, CHO), 7.87 (2H, d, J 8.9 Hz, ArH), 7.40-7.24 (3H, m, ArCl2H), 7.12 (2H, d, J 8.7 Hz, ArH) and 5.36 (2H, s, ArCH2OAr); m/z (ESI, 60V) 281 (M++1); Found: C, 59.76; H, 3.57. C14H10O2Cl2 requires C, 59.81; H, 3.59%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329362B1
Source datasetuspto-grants-2001_12
ORD IDord-ff4899894a5d4f8e92478e2f2d719978
Source noteuspto-grants-2001_12