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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849666Generated: October 30, 2026

Benzylamine → 1-(1-Benzylamino-1-cyanomethyl)-1-ethoxycarbonylcyclopropane

https://huagongshe.com/reaction/849666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantPotassium CyanideHCID 9032—
ReactantEthyl 1-formylcyclopropanecarboxylateHCID 9964122—
ReactantSodium BisulfiteHCID 23665763—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-(1-Benzylamino-1-cyanomethyl)-1-ethoxycarbonylcyclopropaneHCID 1539104679%

Reaction Conditions

Temperature50 °C

Reaction Steps

An eggplant type flask was charged with 501 mg of ethyl 1-formylcyclopropane-1-carboxylate and 2 ml of water to which were further added 1.13 g of sodium hydrogen sulfite and 345 mg of potassium cyanide. Thereto was added dropwise 564 mg of benzylamine dissolved in 5 ml of ethanol at room temperature, followed by 2.5 hours of stirring the reaction solution at 50° C. After confirming completion of the reaction, the reaction solution was mixed with ice water and extracted with ethyl acetate. Next, the resulting organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and, after removing insoluble matter by filtration, concentrated under a reduced pressure. Thereafter, the resulting residue was subjected to a silica gel column chromatography (hexane:ethyl acetate=3:1) to obtain 717 mg (79%) of the title compound in the form of colorless oil. Spectrum data of the thus obtained oily product coincided with those of the compound of Inventive Example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06013806
Source datasetuspto-grants-2000_01
ORD IDord-eeb04ee6567245c5b3e75c2d2b7f8a4a
Source noteuspto-grants-2000_01