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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268411Generated: November 2, 2026

Dimethyl Sulfoxide → Rac. 2-cyano-4-(5-acetoxy-2-hydroxy-3,4,6,-trimethylphenyl)-butan-2-ol

https://huagongshe.com/reaction/268411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium CyanideHCID 9032—
Reactant6-Acetoxy-2-hydroxy-2,5,7,8-tetramethylchromanHCID 14415666—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductRac. 2-cyano-4-(5-acetoxy-2-hydroxy-3,4,6,-trimethylphenyl)-butan-2-olHCID 21432304—

Reaction Conditions

Temperature15 °C

Reaction Steps

A solution of 26.4 g. (0.1 mol.) of (±)-6-acetoxy-2-hydroxy-2,5,7,8-tetramethylchroman in 200 ml. of dimethylsulfoxide was rapidly stirred as 32.5 g. (0.5 mol.) of granular KCN was added by sifting so that a uniformly dispersed suspension was obtained. The resulting mixture was cooled to 15°C. as 47.0 ml. of 12N aqueous H2SO4 was added over 1.25 hours as the internal temp. was maintained at 20°C. Tlc at this point showed a major, slower-running spot in addition to traces of starting material. The material was poured into diethylether and H2O. The ether solutions were washed with water and brine, dried over NaSO4 and stripped of solvent to yield (±)-2-cyano-4-(5-acetoxy-2-hydroxy-3,4,6-trimethylphenyl)butan-2-ol as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947473
Source datasetuspto-grants-1976_03
ORD IDord-7102941752f74cbe88e88faa0bf131a9
Source noteuspto-grants-1976_03