HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636997Generated: October 31, 2026
Sodium Cyanide → methyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetate
https://huagongshe.com/reaction/1636997
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2-(Chloromethyl)benzoyl chloride | HCID 3016395 | — |
| Catalyst | Quinoline | HCID 7047 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | methyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetate | HCID 9812919 | 97.5% |
Reaction Steps
A mixture of acetonitrile (100 ml), 95% sodium cyanide (6.19 g), 95% cuprous iodide (2.00 g) and quinoline (0.13 g) was stirred at 60° C. A solution of 2-chloromethylbenzoyl chloride (19.0 g) in acetonitrile (100 ml) was added dropwise to the reaction mixture over 3 hours. After completion of the addition, the mixture was stirred at 60° C. for 5 hours. After the reaction mixture was cooled by allowing it to stand, the reaction mixture was diluted with ether, and washed successively with water, a saturated aqueous solution of sodium bicarbonate and water. The ether layer thus obtained was dried over anhydrous sodium sulfate and at the same time decolorized with Norit SX-3. Evaporation of the solvent under reduced pressure gave the crude title compound (17.6 g, purity: about 72% determined by 1H-NMR analysis).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06037495 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-d2314cc2a35b4d80b854c35c96831f15 |
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| Source note | uspto-grants-2000_03 |
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