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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500613Generated: October 28, 2026

Allyl bromide → 3-Allyloxy-2,6-dichloro-benzaldehyde

https://huagongshe.com/reaction/500613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Dichloro-3-hydroxy-benzaldehydeHCID 10442530—
SolventDimethylformamideHCID 6228—
Product3-Allyloxy-2,6-dichloro-benzaldehydeHCID 86612401—

Reaction Steps

2,6-dichloro-3-hydroxybenzaldehyde (960 mg, 5.03 mmol) (Synthesis, 2004, 12, 2062), allyl bromide (431 μL, 5.03 mmol) and potassium carbonate (563 mg, 10.06 mmol) were combined in DMF (5 mL) and stirred at room temperature for 18 hours. The DMF was removed in vacuo and the residue partitioned between diethyl ether (50 mL) and water (30 mL). The layers were separated and the aqueous extracted with diethyl ether (2×30 mL). The combined organic solution was dried over magnesium sulphate and concentrated in vacuo to afford the title compound as a yellow solid which was used without further purification in preparation 75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772223B2
Source datasetuspto-grants-2010_08
ORD IDord-cb8075cf0150448183c394c40d345740
Source noteuspto-grants-2010_08