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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029862Generated: October 25, 2026

Allyl chloride → N-allyl-N-formyl-2-methyl-4-nitroaniline

https://huagongshe.com/reaction/1029862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methyl-4-nitrophenylformamideHCID 3557018—
SolventDimethylformamideHCID 6228—
ProductN-allyl-N-formyl-2-methyl-4-nitroanilineHCID 1572468895%

Reaction Steps

155 g of potassium carbonate were introduced into 500 ml of dimethylformamide. 50 g (0.28 mol) of N-formyl-2-methyl-4-nitroaniline were added to this mixture to give an orange solution, which became blood-red after 128.6 g (136.8 ml, 1.68 mol) of allyl chloride were added. The resultant reaction mixture was stirred overnight and subsequently poured into 1.5 1 of ice water. The crude product which deposited was extracted twice from the aqueous phase with 400 ml of dichloromethane in each case. The two combined dichloromethane phases were washed three times with 500 ml of water in each case, subsequently dried over sodium sulfate and then evaporated, to give 58.3 g of N-allyl-N-formyl-2-methyl-4-nitroaniline (yield: 95%) as an orange oil which crystallized in the refrigerator. The product had a melting point of 56° C. and the following physical/chemical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05103060
Source datasetuspto-grants-1992_04
ORD IDord-c9401284c2b3438ba0260d3441315445
Source noteuspto-grants-1992_04