HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720568Generated: October 31, 2026
1,2-Dichloroethane → HCID 22419013, compound
https://huagongshe.com/reaction/1720568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Monomethylamine methanol | HCID 57454252 | — |
| Reactant | HCID 88287593 | HCID 88287593 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22419013 | HCID 22419013 | 42.8% |
Reaction Steps
1,2-Dichloroethane (1 ml), thionyl chloride (0.03 g, 0.28 mmol) and dimethylformamide (DMF)(0.01 ml) were added to (E)-2-(2-chloro-3-pyridyloxymethyl)-α-methoxyiminophenylacetic acid (0.05 g, 0.14 mmol). The mixture was stirred under reflux for 1 hour. To the reaction mixture was added 40% methylamine/methanol solution (1 ml) under ice-cooling. The mixture was stirred at 0° C. for 1 hour. After completion of the reaction, water (100 ml) was added, and the mixture was extracted with methylene chloride (50 ml) twice. The methylene chloride layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to give (E)-2-[2-(2-chloro-3-pyridyloxymethyl)phenyl]-2-methoxyimino-N-methylacetamide (0.02 g, 42.8 %) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05506358 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-a8293d092e944438b7aaff5e6cd7eb91 |
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| Source note | uspto-grants-1996_04 |
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