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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464525Generated: October 25, 2026

Water → 5-(2,5-Dimethoxy-3,4,6-trimethylphenyl)-5-phenylvaleronitrile

https://huagongshe.com/reaction/1464525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropyl EtherHCID 7914—
ReactantSodium CyanideHCID 8929—
Reactant1-Iodo-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-4-phenylbutaneHCID 19088027—
SolventDimethyl SulfoxideHCID 679—
Product5-(2,5-Dimethoxy-3,4,6-trimethylphenyl)-5-phenylvaleronitrileHCID 19088086163%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 4.19 g (5.0 mmole) of 1-iodo-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-4-phenylbutane in dimethylsulfoxide (30 ml) was added 0.74 g (5×3 mmole) of sodium cyanide, and the mixture was stirred at 50° C. for 2 hours. The reaction solution was cooled with ice, and isopropyl ether and water were added to it, followed by stirring. The isopropyl ether layer was separated out, washed with aqueous sodium chloride solution, dried (magnesium sulfate) and evaporated. The residual solution was chromatographed on a silica gel column to perform purification (elution with isopropyl ether/hexane) to thereby give 1.65 g (98%) of 5-(2,5-dimethoxy-3,4,6-trimethylphenyl)-5-phenylvaleronitrile. Its typical physical properties and nuclear magnetic resonance spectrum data are shown in Table 14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304658
Source datasetuspto-grants-1994_04
ORD IDord-316c513b3521443883167070cb77e4ff
Source noteuspto-grants-1994_04