HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463896Generated: October 30, 2026
Dimethylformamide → HCID 20265424, compound
https://huagongshe.com/reaction/463896
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 13424156 | HCID 13424156 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 20265424 | HCID 20265424 | — |
Reaction Steps
A solution of N-[3-(4-chlorobenzoyl)-5-methylisoxazol-4-yl]-bromoacetamide of Example Vc (4.26 g, 15.5 mmoles) in dimethylformamide (DMF) (40 ml) was added to a suspension of hexane-washed sodium hydride (0.67 g, 14 mmoles, 50% oil dispersion) in DMF (40 ml) at 5° C. After warming to 20° C., methyl iodide (1.06 ml, 17 mmoles) was added. The reaction solution was Poured into dilute sodium bicarbonate (600 ml) with stirring. The precipitate was extracted with ethyl acetate, the organic solution was washed with water, saturated sodium chloride, and dried (sodium sulfate). Concentration gave a residue (5.5 g) which was chromatographed by high pressure liquid chromatography (HPLC) (8% ethyl acetate:dichloromethane) to give a solid that was pulverized to yield 3.0 g (66%) of a powder, melting point 133°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04544753 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-ebe92f51a76447ac94b839ac6fa106ea |
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| Source note | uspto-grants-1985_10 |
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