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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985414Generated: November 3, 2026

N-Formylmorpholine → 5-(Dimethoxymethyl)-2-fluorobenzaldehyde

https://huagongshe.com/reaction/1985414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FormylmorpholineHCID 20417—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-4-(dimethoxymethyl)-1-fluorobenzeneHCID 22260864—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-(Dimethoxymethyl)-2-fluorobenzaldehydeHCID 222607048%

Reaction Conditions

Temperature-60 °C

Reaction Steps

6.2 g of 2-Bromo-4-dimethoxymethyl-1-fluorobenzene was dissolved in 65 ml of tetrahydrofuran, and the solution was cooled to −60° C. under a nitrogen gas flow. 18 ml of 1.6M n-Butyl lithium in hexane was added dropwise and the mixture was stirred at −60° C. for 1 hour. 3.3 ml of N-Formylmorpholine was added thereto, and the reaction mixture was allowed to warm to room temperature. The mixture was stirred for 1 hour, then ice-cooled, and treated with water and ammonium chloride solution, then extracted with ethylacetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and evaporated. The residue was subjected to silica gel column chromatography, to give 2.8 g of the title compound (8% ethyl acetate-hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544835B2
Source datasetuspto-grants-2009_06
ORD IDord-8b403390309646caa5dcc6ba0835f738
Source noteuspto-grants-2009_06