HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756752Generated: October 30, 2026
Dimethyl Sulfate → 2-Phenoxy-alpha-methoxyiminobenzyl cyanide
https://huagongshe.com/reaction/1756752
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Phenoxy-alpha-hydroxyiminobenzyl cyanide | HCID 85321215 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Phenoxy-alpha-methoxyiminobenzyl cyanide | HCID 54165365 | 108.2% |
Reaction Steps
Potassium carbonate (3.11 g, 0.023 mol) and acetone (60 ml) were added to 2-phenoxy-α-hydroxyiminobenzyl cyanide (E/Z=11/89)(7.15 g, 0.03 mol). The mixture was stirred for 5 minutes. Then dimethyl sulfate (5.68 g, 0.045 mol) was added, and the mixture was stirred at room temperature for 18 hours. After completion of the reaction, the resulting insoluble materials were removed. To the residue obtained after concentration under reduced pressure, toluene (60 ml) and 1N aqueous sodium hydroxide solution (60 ml) were added. The mixture was stirred at room temperature for 1 hour. After stirring, water (60 ml) was added. The mixture was extracted with toluene (100 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel chromarography (ethyl acetate/n-hexane) to give 2-phenoxy-α-methoxyiminobenzyl cyanide (6.28 g, Yield: 83.0%, E/Z=7/93).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05442063 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-0aa9f55a436b4263a988af40623bf436 |
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| Source note | uspto-grants-1995_08 |
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