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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309605Generated: November 4, 2026

Acetone Cyanohydrin → HCID 13983073, compound

https://huagongshe.com/reaction/2309605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetone CyanohydrinHCID 6406—
ReactantTriethylamineHCID 8471—
Reactant2-Nitrobenzoyl chlorideHCID 11875—
ReactantHCID 18411288HCID 18411288—
SolventDichloromethaneHCID 6344—
ProductHCID 13983073HCID 13983073—

Reaction Steps

Triethylamine (3.4 ml, 0.025 mole) was added dropwise to a methylene chloride solution of 2-nitrobenzoyl chloride (3.5 g, 0.019 mole) and 5,5-dimethylcyclohexanedione (2.4 g, 0.019 mole). After stirring for one hour at room temperature an additional 3 equivalents of triethylamine and 0.4 ml acetone cyanohydrin were added. The solution was stirred for 2.5 hours, then washed with 2N HCl and extracted with 5% potassium carbonate solution. The basic extracts were acidified with 2N HCl and extracted with ether. The ether portion was washed with saturated sodium chloride solution, dried over anhydrous MgSO4 and concentrated under vacuum. The residue was recrystallized from ethyl acetate yielding 2.0 g of the desired compound (m.p. 130°-133° C.) which was identified as such by nuclear magnetic resonance, infrared and mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695673
Source datasetuspto-grants-1987_09
ORD IDord-b6c5311f532f4cfb9cb87bb303d6f290
Source noteuspto-grants-1987_09