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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392587Generated: October 30, 2026

Water → HCID 18979554, compound

https://huagongshe.com/reaction/2392587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3,4-DihydroxybenzonitrileHCID 87065—
ReactantHCID 18979499HCID 18979499—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18979554HCID 18979554—

Reaction Conditions

Temperature-25 °C

Reaction Steps

0.9 g of triethylamine and then 0.5 g of methanesulphonyl chloride were added dropwise at -25° C. while stirring to a solution of 2.0 g of 4-(8-acryloyloxyoctyloxy)biphenyl-4'-carboxylic acid in 40 ml of tetrahydrofuran. The reaction mixture was stirred at -25° C. for 1 hour, then treated with 0.25 g of 3,4-dihydroxybenzonitrile and 0.05 g of 4-(dimethylamino)pyridine, stirred at room temperature overnight, poured into 100 ml of water and then extracted three times with 50 ml of diethyl ether each time. The organic phases were combined, washed twice with 100 ml of water each time, dried over magnesium sulphate, filtered and the filtrate was concentrated. Chromatographic purification of the residue on silica gel with cyclohexane/ethyl acetate (vol. 8:2) and two-fold recrystallization from a cyclohexane/ethyl acetate mixture (vol. 8:2) of the fractions which were pure according to thin-layer chromatography gave 1.0 g of 3,4-bis[4-(8-acryloyloxyoctyloxy)biphenyl-4'-carbonyloxy]benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05800733
Source datasetuspto-grants-1998_09
ORD IDord-bcec63a8d5c540ef94a9d2d0399c143b
Source noteuspto-grants-1998_09