Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392586Generated: October 30, 2026

4-Hydroxybenzaldehyde → HCID 18979467, compound

https://huagongshe.com/reaction/2392586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-{[8-(Acryloyloxy)octyl]oxy}benzoic acidHCID 54113072—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18979467HCID 1897946751.8%

Reaction Conditions

Temperature-25 °C

Reaction Steps

0.6 g of triethylamine and then 0.4 g of methanesulphonyl chloride were added dropwise at -25° C. while stirring to a solution of 1.0 g of 4-(8-acryloyloxyoctyloxy)benzoic acid in 40 ml of tetrahydrofuran. The reaction mixture was stirred at -25° C. for 1 hour, then treated with 0.20 g of 4-hydroxybenzaldehyde and 0.03 g of 4-(dimethylamino)pyridine in 40 ml of tetrahydrofuran, 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 0.6 g of 3,4-bis(4-[8-acryloyloxyoctyloxy]phenylcarbonyloxy)benzaldehyd; m.p. (C-I) 56° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05800733
Source datasetuspto-grants-1998_09
ORD IDord-fff96cf85ed14afc9e548e45406cb29b
Source noteuspto-grants-1998_09