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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245337Generated: October 29, 2026

Acetonitrile → HCID 178433102, compound

https://huagongshe.com/reaction/245337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantAcetone CyanohydrinHCID 6406—
ReactantTriethylamineHCID 8471—
ReactantHCID 58453093HCID 58453093—
ProductHCID 178433102HCID 17843310293%

Reaction Steps

To acetonitrile (5 ml) solution of 1-methyl-1H-pyrazole-5-yl 2-methyl-6-(1H-1,2,4-triazol-1-yl)nicotinate (0.19 g, 0.65 mmol) and triethylamine (0.13 g, 1.29 mmol) , a catalytic amount of acetone cyanohydrin was added. The obtained solution was stirred at room temperature around the clock. Volatile materials were evaporated under reduced pressure from the obtained reaction solution, and the obtained residue was made acidic with citric acid aqueous solution, and was extracted with ethyl acetate. After washing the obtained organic layer with water, the organic layer was dried with magnesium sulfate and concentrated to obtain the desired product (0.18 g, yield 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658798B2
Source datasetuspto-grants-2014_02
ORD IDord-cf6f2f04372548878a0f820d5df82279
Source noteuspto-grants-2014_02