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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218093Generated: October 26, 2026

2-fluoro-N,3-dimethoxy-N-methylbenzamide → 2-Fluoro-3-methoxybenzaldehyde

https://huagongshe.com/reaction/2218093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-fluoro-N,3-dimethoxy-N-methylbenzamideHCID 17981929—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-3-methoxybenzaldehydeHCID 377446385%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-fluoro-3,N-dimethoxy-N-methyl-benzamide (2.30 g, 10.8 mmol) in THF (20 mL) at −78° C. was added 1M DEBAL-H in toluene.(12 mL, 12 mmol). The reaction stirred at −78° C. for 3 h and then the remaining 1M DIDAL-H in toluene (4.2 mL, 4.2 mmol) was added to the reaction. The reaction was allowed to stir at −78° C. for 30 min and was then warmed to rt. The reaction was quenched slowly with saturated aqueous NH4Cl. The organic phase was separated and the aqueous phase was extracted with 2×50 mL ethyl acetate. The combined organic phases were washed successively with 1N HCl and brine. The organic phase was dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography eluting silica gel with EtOAc:hexane [0:100 to 1:1] to yield the title compound (1.41 g, 85%): δH (300 MHz, CDCl3): 10.38 (1H, s), 7.43-7.40 (1H, m), 7.24-7.15 (2H, m), 3.95 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410982B2
Source datasetuspto-grants-2008_08
ORD IDord-7c7e92e8c78a4ad8abe2a84d170b9a94
Source noteuspto-grants-2008_08