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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230123Generated: October 26, 2026

Dimethylformamide → 2-(4-formylphenoxy)-N-methylacetamide

https://huagongshe.com/reaction/230123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantAcetic acid, 2-(4-formylphenoxy)-HCID 89177—
SolventDichloromethaneHCID 6344—
Product2-(4-formylphenoxy)-N-methylacetamideHCID 15270519—

Reaction Steps

2-(4-formylphenoxy)acetic acid was suspended in 20 mL of DCM at 0° C., and 0.5 mL of DMF was added followed by the dropwise addition of oxalyl chloride. The solution was allowed to warm to room temperature with stirring until gas evolution stopped and the solution was homogeneous. The solution containing the crude acid chloride was concentrated under vacuum and the residue resuspended in DCM, cooled to 0° C., and methylamine and DIEA were added. The mixture was allowed to warm to room temperature with stirring over 12 hours. The reaction mixture was then poured into 5% HCl, washed 3 times with EtOAc, dried over sodium sulfate, filtered and concentrated to a thick brown oil which was purified by column using DMC/MeOH to afford 2-(4-formylphenoxy)-N-methylacetamide (9) as an off white solid. NMR (CDCl3, 400 mHz), d═9.9 (1H, s), 7.88 (2H, d, J=8.6 Hz), 7.04 (2H, d, J=8.6 Hz), 6.6-6.5 (1H, BS, 4.54 (2H, s), 2.93 (3H, d, J=4.7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566716B2
Source datasetuspto-grants-2009_07
ORD IDord-42d66c4839a14e6cbde5bd17cf1f9a11
Source noteuspto-grants-2009_07