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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270091Generated: October 26, 2026

Dimethylformamide → 3-Chloro-5-methoxybenzaldehyde

https://huagongshe.com/reaction/1270091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
Reactant3,5-DichloroanisoleHCID 36588—
ReactantMagnesiumHCID 5462224—
Catalyst1,2-DibromoethaneHCID 7839—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-5-methoxybenzaldehydeHCID 2190463354%

Reaction Conditions

Temperature0 °C

Reaction Steps

3,5-Dichloroanisole (74.0 g, 419 mmol) in THF (200 mL) was added dropwise to magnesium metal (14.2 g, 585 mmol, pre-washed with 0.5 N HCl) in THF (100 mL) at 25° C. After the addition, 1,2-dibromoethane (3.9 g, 20.8 mmol) was added dropwise. The resultant dark brown mixture was heated at reflux for 3 h. The mixture was cooled to 0° C., and N,N-dimethylformamide (60 mL) was added in one portion. The mixture was partitioned with diethyl ether (3×400 mL) and 6N HCl (500 mL). The combined organic extracts were washed with brine (300 mL), dried (Na2SO4), filtered and concentrated in vacuo to give an oil. Flash chromatography (2×) on silica gel eluting with Hex:EtOAc (4:1) afforded the sub-title compound (38.9 g, 54%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202236B2
Source datasetuspto-grants-2007_04
ORD IDord-7dbaf989b0d44317adc016c9e5f0d153
Source noteuspto-grants-2007_04