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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917533Generated: October 31, 2026

Dimethylformamide → HCID 58963161, compound

https://huagongshe.com/reaction/917533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant5-Bromo-7-ethyl-3-methyl-1-benzofuranHCID 58963156—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58963161HCID 5896316141.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

5-Bromo-7-ethyl-3-methylbenzofuran 31 (21.25 g, 89 mmoles) was dissolved in dry THF (470 ml) and cooled to −78° C. under a nitrogen atmosphere. Sec-butyl lithium (69.8 ml of a 1.4 M solution, 98 mmoles) was added drop wise to the cooled reaction. The reaction mixture turned a reddish color. Dimethylformamide (51.6 ml, 666 mmoles) was added to the reaction at −78° C. The reaction was allowed to warm to room temperature and stirred overnight. The reaction was poured into 800 ml of ice/ethyl acetate and the organic layer separated. The aqueous layer was washed with ethyl acetate and the combined organic layer washed with water. The solution was dried over sodium sulfate, filtered, and the solvent removed in vacuo. The crude product was purified by flash chromatography (750 g silica, 8% ethyl acetate in hexanes) to yield 7.02 g of 7-ethyl-3-methylbenzofuran-5-carbaldehyde 32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273886B2
Source datasetuspto-grants-2007_09
ORD IDord-2b62800637a6488da2c6c49ba76fdfa5
Source noteuspto-grants-2007_09