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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985912Generated: November 2, 2026

2,3-Dimethylbenzaldehyde → HCID 44815677, compound

https://huagongshe.com/reaction/1985912

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DimethylbenzaldehydeHCID 34224—
Reactant1-(diethoxymethyl)-1H-imidazoleHCID 3849535—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44815677HCID 4481567772%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-(diethoxymethyl)-1H-imidazole (698 mg, 4.10 mmol) in anhydrous tetrahydrofuran (7 ml), at −78° C., was added n-butyllithium (2.5 M in hexane, 1.64 ml, 4.1 mmol). The reaction mixture was stirred at −78° C. for 1 h, before addition of a solution of 2,3-dimethylbenzaldehyde (500 mg, 3.73 mmol) in tetrahydrofuran (3 ml). The reaction mixture was stirred at −78° C. for 2 h, warmed to room temperature and quenched with ice cold hydrochloric acid (4M, 20 ml). The reaction mixture was concentrated in vacuo and to the residue was added water (20 ml). The solution was extracted with diethyl ether (2×20 ml) and the aqueous layer was basified by addition of solid sodium hydrogen carbonate. This solution was extracted with ethyl acetate (3×20 ml) and the combined organic phases were dried (MgSO4) and concentrated in vacuo to give the title compound (543 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547718B2
Source datasetuspto-grants-2009_06
ORD IDord-1f3e8a51decb450d923a81d929e65d02
Source noteuspto-grants-2009_06