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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700725Generated: November 1, 2026

Dimethylformamide → 5-Chloro-2-fluorobenzaldehyde

https://huagongshe.com/reaction/1700725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzene, 1-chloro-4-fluoro-HCID 9604—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-Chloro-2-fluorobenzaldehydeHCID 277358664.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1.6M butyllithium in hexane (32 ml) was added anhydrous tetrahydrofuran (100 ml), and then added dropwise 2,2,6,6-tetramethylpiperidine (8.4 ml) at −70° C. or less. To the mixture was added dropwise a solution of 1-chloro-4-fluorobenzene (6.5 g) in anhydrous tetrahydrofuran (20 ml), and the mixture was stirred at −70° C. or less for 2 hours. To the mixture was added dropwise a solution of dimethylformamide (6.5 g) in tetrahydrofuran (15 ml), and the mixture was allowed to stand to warm up to 0° C. The reaction solution was poured into ice-water and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated to give oil of 5-chloro-2-fluorobenzaldehyde (5.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-b386910a3ba54cef97117322479752e3
Source noteuspto-grants-2002_02