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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301471Generated: November 1, 2026

Dimethylformamide → 2-Fluoro-3-(1-undecynyl)benzaldehyde

https://huagongshe.com/reaction/2301471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
Reactant2-(1-Undecynyl)fluorobenzeneHCID 18373021—
ReactantButyllithiumHCID 178418339—
SolventDichloromethaneHCID 6344—
Product2-Fluoro-3-(1-undecynyl)benzaldehydeHCID 1837305745.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-(1-undecynyl)fluorobenzene (7.00 g) and tetrahydrofuran (70 ml) was added slowly n-butyllithium (1.6 M, 17.8 ml) at −78° C. The reaction mixture was stirred at −78° C. for 1.5 hrs. Dimethylformamide (2.28 ml) was added slowly, and the solution was allowed to warm to room temperature over 1 hr, with stirring. Methylene chloride (300 ml) was added, and the solution was washed with 50% hydrochloric acid. The aqueous phase was extracted with methylene chloride. The extracts were combined, dried over anhydrous magnesium sulfate, filtered, and the filtrate was evaporated. The residue was chromatographed on silica (250 g), eluting with hexane followed by ethyl acetate/hexane (1:4). The appropriate fractions were collected and evaporated to provide 3.53 g (45.2%) of product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500849B1
Source datasetuspto-grants-2002_12
ORD IDord-23ca51d9c31645578f6d1d8afec50fe2
Source noteuspto-grants-2002_12