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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161764Generated: October 29, 2026

Benzyl Bromide → 4-(Benzyloxy)-2,6-dichlorobenzaldehyde

https://huagongshe.com/reaction/1161764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Dichloro-4-hydroxybenzaldehydeHCID 528382—
SolventDimethylformamideHCID 6228—
Product4-(Benzyloxy)-2,6-dichlorobenzaldehydeHCID 11150210—

Reaction Steps

Treat a mixture of 2,6-dichloro-4-hydroxy-benzaldehyde (250 g, 1.3 mol) and potassium carbonate (361.8 g, 2.62 mol) in 2 L dimethylformamide with benzyl bromide (268.64 g, 1.57 mol). Stir the reaction at room temperature for 1 hour. Filter off solids and pour into 12 L of water. Filter off solid, wash several times with water, air dry and dissolve in ethyl acetate. Dry over magnesium sulfate, filter and concentrate under vacuum to ˜1.5 L. Allow to sit overnight then filter. Wash solid with minimal amount of hexane and vacuum dry. Concentrate the filtrate under vacuum and triturate with hexane to yield a second crop of product which when combined with the first crop equals 245 g white crystals. Repeat to obtain a 3rd crop of 80 g as a light-tan powder (88% overall yield): 1H NMR (400 MHz, DMSO-d6) δ 10.26 (s, 1H), 7.43 (m, 5H), 7.28 (s, 2H), 5.25 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820659B2
Source datasetuspto-grants-2010_10
ORD IDord-739837224d77445ea27e53b00e05b325
Source noteuspto-grants-2010_10