HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224498Generated: October 31, 2026
Dimethylformamide → N-isopropyl-4'-chloro-2-methylacetoacetanilide
https://huagongshe.com/reaction/224498
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-isopropyl-4'-chloroacetoacetanilide | HCID 20297524 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-isopropyl-4'-chloro-2-methylacetoacetanilide | HCID 20297522 | 80% |
Reaction Steps
A one liter reaction flask equipped with a power stirrer, condener, drying tube, thermometer and nitrogen inlet tube was charged with 48.5 g (0.19 mole) of N-isopropyl-4'-chloroacetoacetanilide and 145 ml of dry dimethylformamide. With efficient stirring in a nitrogen atmosphere, portionwise addition of 7.2 g of 57% sodium hydride in mineral oil (0.17 mole) was completed in one hour (excessive foaming). Methyl iodide (24.1 g, 0.17 mole) was added dropwise and the reaction mixture was stirred for two hours at ambient temperature. The mixture was poured into one liter of cold water and stirred. The organic material was extracted into toluene and the latter was water washed. Most of the toluene was removed on the rotary evaporator. Hexane was added which caused the mass to crystallize. There was obtained 36.4 g (80%) of white material, M.P. 77°-79°. N.M.R. (CDCl3) ∂0.9-1.4 (CH3, 9 protons), 2.0 (0=C--CH3), 2.9-3.2 (CH), 4.7-5.2 (CH, isopropyl), 6.9-7.5. (aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04232163 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-6c275ddd54634c66af47631b8fef69a0 |
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| Source note | uspto-grants-1980_11 |
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