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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505009Generated: October 27, 2026

Dimethylformamide → 3-Chloro-5-methoxybenzaldehyde

https://huagongshe.com/reaction/505009

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 numberUS07781424B2
Source datasetuspto-grants-2010_08
ORD IDord-cc3046cd0f33442e9fd5e9760d1ffc81
Source noteuspto-grants-2010_08