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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant2-(Chloromethyl)benzoyl chlorideHCID 3016395—
CatalystQuinolineHCID 7047—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Productmethyl(2E)-[2-(chloromethyl)phenyl](methoxyimino)acetateHCID 981291997.5%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06037495
Source datasetuspto-grants-2000_03
ORD IDord-d2314cc2a35b4d80b854c35c96831f15
Source noteuspto-grants-2000_03