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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344732Generated: October 26, 2026

4-Methoxyphenol → 2-(4-Methoxyphenoxy)-2-methylpropanal

https://huagongshe.com/reaction/344732

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
ReactantSodium HydroxideHCID 14798—
Reactant1,1-Dichloro-2-hydroxy-2-methylpropaneHCID 10964627—
CatalystHexadecyltrimethylammonium BromideHCID 5974—
SolventDiethyl EtherHCID 3283—
Product2-(4-Methoxyphenoxy)-2-methylpropanalHCID 15192047—

Reaction Steps

A solution of 4-methoxyphenol, (21.72 g, 0.175 mol), in aqueous sodium hydroxide solution, (5.8M, 30 ml), was treated with cetyltrimethyl ammonium bromide, (0.255 g, 0.7 mmol), followed by a solution of 1,1-dichloro-2-hydroxy-2-methylpropane, (5.01 g, 35 mmol), in ether, (70 ml). The mixture was stirred under an argon atmosphere for 18 hours then diluted with ether, (100 ml), and extracted with aqueous sodium hydroxide solution, (2M, 4×50 ml), to remove unreacted phenol. The combined aqueous extracts were extracted with ether, (100 ml), and the organic phase was washed with aqueous sodium hydroxide solution, (2M, 50 ml), and water, (100 ml). The combined organic extracts were dried, (MgSO4), concentrated and purified by flash column chromatography, eluting with ethyl acetate/hexane, (10%, v/v), to give 2-(4-methoxyphenoxy)-2-methylpropanal, (3.61 g), as an oil; NMR: 1.36(6H,s), 3.76(3H,s), 6.7-6.9(4 H,m) and 9.85(1H,s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053415
Source datasetuspto-grants-1991_10
ORD IDord-90a5560f32674f5fbefba900c71ff540
Source noteuspto-grants-1991_10