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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342048Generated: October 31, 2026

Hydrochloric Acid → HCID 70145902, compound

https://huagongshe.com/reaction/342048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CyanideHCID 9032—
ReactantEthyl 1-formylcyclopropanecarboxylateHCID 9964122—
Reactant(S)-1-Phenyl-2-(p-tolyl)ethylamineHCID 10160531—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 70145902HCID 7014590267.4%

Reaction Steps

An eggplant type flask was charged with 133 mg of potassium cyanide, 1.0 g of (S)-1-phenyl-2-p-tolylethylamine and 1 ml of water. After adding 146 mg of ethyl 1-formylcyclopropane-1-carboxylate dissolved in 2.5 ml of ethanol, dropwise at room temperature, the resulting mixture was further mixed with 0.2 ml of concentrated hydrochloric acid, and stirred for 1 hour at the same temperature and then for 2 hours 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 water and saturated brine, and dried over anhydrous magnesium sulfate and, after removing insoluble matter by filtration, the solvent was evaporated under a reduced pressure. Thereafter, the resulting residue was subjected to a silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain 251 mg (67%) of a diastereomer mixture in the form of colorless oil. Formation ratio of the two diastereomers was found to be 4:1 based on the integral ratio of NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856518
Source datasetuspto-grants-1999_01
ORD IDord-eecdd886547243ab90db5983e6a37238
Source noteuspto-grants-1999_01