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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392584Generated: October 30, 2026

4-Hydroxybenzaldehyde → HCID 18979539, compound

https://huagongshe.com/reaction/2392584

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-{[8-(Acryloyloxy)octyl]oxy}benzoic acidHCID 54113072—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 18979539HCID 1897953983.3%

Reaction Steps

3.9 g of N,N'-dicyclohexylcarbodiimide were added at 0° C. within 15 minutes while stirring to a solution of 1.9 g of 4-hydroxybenzaldehyde, 5.0 g of 4-[8-acryloyloxyoctyloxy]benzoic acid and 0.1 g of 4-(dimethylamino)pyridine in 100 ml of dichloromethane. The reaction mixture was stirred at room temperature overnight, 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 ethyl acetate of the fractions which were pure according to thin-layer chromatography gave 5.5 g of 4-(4-[8-acryloyloxyoctyloxy]phenylcarbonyloxy)benzaldehyde; m.p. 73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05800733
Source datasetuspto-grants-1998_09
ORD IDord-70d655116db5408b80f61c1ba14ec0d5
Source noteuspto-grants-1998_09