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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355600Generated: October 26, 2026

Water → 1-[4'-(4"-Acryloxybutoxy)benzoyloxy]-4-[4'-(2"-acryloxyethoxy)-benzoyloxy]benzene

https://huagongshe.com/reaction/355600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantOxalyl chlorideHCID 65578—
Reactant4-[4'-(4-Acryloxybutoxy)benzoyloxy]phenolHCID 15218597—
Reactant4-(2-Prop-2-enoyloxyethoxy)benzoic acidHCID 15544605—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
Product1-[4'-(4"-Acryloxybutoxy)benzoyloxy]-4-[4'-(2"-acryloxyethoxy)-benzoyloxy]benzeneHCID 1521859883.3%

Reaction Steps

Oxalyl chloride (10 ml) is added at 0° C. to 4-(2'-acryloxyethoxy)-benzoic acid (4.3 g; 16.3 mmol), and the mixture is stirred until the evolution of gas subsides (30 min). The excess oxalyl chloride is removed by distillation in a water-pump vacuum, the acid chloride is taken up in toluene (10 ml), the toluene solution is added at 0° C. to a solution of (3) (5.8 g; 16.3 mmol) in pyridine (10 ml) and toluene (5 ml), and the mixture is subsequently stirred at room temperature for 13 hours. The reaction mixture is then transferred into water (200 ml), and the mixture is extracted twice with dichloromethane (50 ml each time). The organic extracts are dried using calcium chloride, hydroquinone (50 mg) is added to the filtrate, and the mixture is evaporated in a water-pump vacuum. The residue is chromatographed on silica gel (toluene/ethyl acetate (5:1), giving 7.8 g (83%) of (4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05833880
Source datasetuspto-grants-1998_11
ORD IDord-ede8c3aa81184a1dbe1c2f1dae99382b
Source noteuspto-grants-1998_11