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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016776Generated: October 30, 2026

Dimethylformamide → 3-Ethyl-4-methoxybenzaldehyde

https://huagongshe.com/reaction/1016776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHexaneHCID 8058—
Reactant4-Bromo-2-ethyl-1-methoxybenzeneHCID 13301602—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Ethyl-4-methoxybenzaldehydeHCID 2203977242.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 4-bromo-2-ethyl-1-methoxybenzene (J. Chem. Soc., Perkin Trans. 1, 1987, 1423; 2.13 g, 9.9 mmol) in THF (30 ml) was cooled to −78° C. A 1.6M solution of n-BuLi in hexane (7.42 ml, 11.9 mmol) was added slowly and the mixture was stirred for 1.5 h. at −78° C. The mixture was warmed slowly to −10° C. and subsequently again cooled to −78° C. DMF (2.29 ml, 29.7 mmol) was added slowly and the mixture was stirred for 1 h. at −78° C. and for 1 h. at 0° C. The reaction mixture was poured into ice-cold 3M HCl and extracted with diethyl ether. The organic phase was dried and filtered, and the filtrate was concentrated. The residue was purified by chromatography (SiO2, hexane/EtOAc 8:1=>2:1). There were obtained 690 mg (42%) of 3-ethyl-4-methoxy-benzaldehyde as a yellowish liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476264B2
Source datasetuspto-grants-2002_11
ORD IDord-d35dbbf430d441478259eb0344af3100
Source noteuspto-grants-2002_11