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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603167Generated: October 31, 2026

2,4-Dihydroxybenzaldehyde → 2-hydroxy-4-(3methylbut-2-enyloxy)benzaldehyde

https://huagongshe.com/reaction/1603167

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DihydroxybenzaldehydeHCID 7213—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Butene, 1-bromo-3-methyl-HCID 70092—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventEthyl AcetateHCID 8857—
Product2-hydroxy-4-(3methylbut-2-enyloxy)benzaldehydeHCID 1086746717.3%

Reaction Steps

A solution of 6 g (0.11 mol) of potassium hydroxide, 22.7 g (0.1 mol) of benzyltriethylammonium chloride, and 14 g (0.1 mol) of 2,4-dihydroxybenzaldehyde was concentrated in vacuo. The residue was suspended in 100 ml of ethyl acetate and 11.7 ml (0.1 mol) of dimethylallyl bromide was slowlv added to the solution. The mixture was extracted with 100 ml of water, and the organic phase was dried and concentrated in vacuo to give 3.568 g of a residue, from which 4.738 g (20%) of 4-(3-methyl)-but-2-enyloxy-2-hydroxybenzaldehyde identical to that previously described by S. Khan, and M. Krishnamurti in Indian J. Chem. 22B (1983), 276 was purified by column chromatography over silica gel 60 (Merck 0.063-0.200 mm, 200 g) using petroleum ether-ethyl acetate (9:1) as an eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05985935
Source datasetuspto-grants-1999_11
ORD IDord-5e2fcd4e4b66447baf30e2a412b4e875
Source noteuspto-grants-1999_11