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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385031Generated: October 25, 2026

Acetone Cyanohydrin → HCID 178463102, compound

https://huagongshe.com/reaction/1385031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetone CyanohydrinHCID 6406—
ReactantSodium CarbonateHCID 10340—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant8-bromoquinoline-5-carboxylic AcidHCID 11021363—
ReactantHCID 178418331HCID 178418331—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 178463102HCID 178463102—

Reaction Steps

1.00 g of 8-bromoquinoline-5-carboxylic acid, 0.44 g of 1-ethyl-5-hydroxypyrazole and 0.80 g of dicyclohexylcarbodiimide were stirred in 15 ml of acetonitrile at room temperature. After the addition of 0.2 ml of acetone cyanohydrin and 0.60 g of triethylamine, stirring was continued for 1.5 hours and the mixture was then poured into aqueous sodium carbonate solution. The alkaline phase was washed with ethyl acetate and diethyl ether and then acidified. The precipitate was filtered off under suction and the aqueous phase was extracted with ethyl acetate. This organic phase was dried and concentrated. The residue and the precipitate were combined.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262074B1
Source datasetuspto-grants-2001_07
ORD IDord-9fdd006d23c84e68816f4a08d800cf40
Source noteuspto-grants-2001_07