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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585114Generated: October 26, 2026

Water → (E)-3-(3-t-Butyl-4-hydroxyphenyl)-2-(4-fluorophenylsulfonyl)acrylonitrile

https://huagongshe.com/reaction/1585114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(4-Fluorobenzenesulfonyl)acetonitrileHCID 565732—
Reactant3-(tert-Butyl)-4-hydroxybenzaldehydeHCID 3017618—
SolventEthanolHCID 702—
Product(E)-3-(3-t-Butyl-4-hydroxyphenyl)-2-(4-fluorophenylsulfonyl)acrylonitrileHCID 2200056782.2%

Reaction Steps

The reaction mixture of 178.0 mg of 3-t-butyl-4-hydroxybenzaldehyde and 219.0 mg of (4-fluorobenzenesulphonyl)acetonitrile in 2.0 mL of ethanol containing 0.01 mL piperidine was refluxed for 4 h and cooled down. To the above reaction mixture was added water and then the aqueous layer was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated. The resulting residue was purified on silica gel column eluting with ethyl acetate-hexane (1:6) to give 295.0 mg of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935993
Source datasetuspto-grants-1999_08
ORD IDord-3c9d45100f354a878e2c4d6e1ca75a87
Source noteuspto-grants-1999_08