HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414253Generated: November 1, 2026
Methyl iodide → 2-[4-Chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-methoxyiminoacetonitrile
https://huagongshe.com/reaction/2414253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2-[4-Chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-hydroxyiminoacetonitrile | HCID 86759549 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[4-Chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-methoxyiminoacetonitrile | HCID 86759550 | 47.5% |
Reaction Steps
0.36 g of 2-[4-chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-hydroxyiminoacetonitrile and 0.54 g of a 28% sodium methylate methanol solution were added to 5 ml of methanol, and 0.49 g of methyl iodide was added thereto, followed by stirring at room temperature for 24 hours. The reaction solution was vacuum concentrated, the solvent was distilled off, water was added to the residue, extraction with ethyl acetate was carried out, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (Wakogel C-200, eluent: hexane/ethyl acetate=4/1-5/1) to obtain 0.18 g of 2-[4-chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-methoxyiminoacetonitrile as colorless crystals (m.p. 104-107° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06812229B1 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-1707d261c467416fb1b0d704048b667a |
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| Source note | uspto-grants-2004_11 |
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