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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methyl-4-nitrophenylformamide | HCID 3557018 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-allyl-N-formyl-2-methyl-4-nitroaniline | HCID 15724688 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05103060 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-c9401284c2b3438ba0260d3441315445 |
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| Source note | uspto-grants-1992_04 |
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