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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301464Generated: October 30, 2026

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

https://huagongshe.com/reaction/2301464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-(1-Dodecynyl)fluorobenzeneHCID 18373058—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Fluoro-3-(1-dodecynyl)benzaldehydeHCID 1837306191%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 7.00 g (27.0 mmol) of 2-(1-dodecynyl)fluorobenzene in tetrahydrofuran (60 ml) at −78° C. was added slowly sec-butyllithium (1.3 M, cyclohexane) (21 ml). The mixture was stirred at −78° C. for 30 min, and dimethylformamide (2.8 ml) was added dropwise. The mixture was stirred for 5 min at −78° C. and allowed to warm to room temperature. The mixture was diluted with ethyl acetate and washed with water. The organic phase was separated, dried over anhydrous magnesium sulfate, filtered, and the filtrate concentrated in vacuo. The residue was flash chromatographed on silica gel (eluted with ethyl acetate/heptane/1:10). The appropriate fractions were collected and evaporated. The residue was chromatographed a second time over silica gel (eluted with dichloromethane) to afford 7.10 g (91%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500849B1
Source datasetuspto-grants-2002_12
ORD IDord-0a8a0a4b4e7a4135a423a8f62f4d7924
Source noteuspto-grants-2002_12