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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722895Generated: November 1, 2026

Potassium Cyanide → 3-Carbobenzoxyamino-2-hydroxy-5-methylhexanenitrile

https://huagongshe.com/reaction/1722895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantN-carbobenzoxy-L-leucinalHCID 10911911—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-Carbobenzoxyamino-2-hydroxy-5-methylhexanenitrileHCID 1384862981.6%

Reaction Steps

A solution of 3.43 g of sodium bisulfite in 20 ml of water was added to 2.81 g of N-carbobenzoxy-L-leucinal, and the mixture was stirred under ice-cooling for 14 hours. To the reaction mixture were added a solution of 1.41 g of potassium cyanide in 50 ml of water and 200 ml of ethyl acetate, and the mixture was stirred at room temperature for 4 hours. The ethyl acetate layer was washed with a saturated sodium chloride aqueous solution, dried over magnesium sulfate, and concentrated under reduced pressure to obtain 2.54 g of 3-carbobenzoxyamino-2-hydroxy-5-methylhexanenitrile as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857650
Source datasetuspto-grants-1989_08
ORD IDord-ee593498200d4266a9b6d9e461d60221
Source noteuspto-grants-1989_08