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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654553Generated: October 31, 2026

Acetonitrile → 4-(6-Acryloyloxyhexyloxy)benzaldehyde

https://huagongshe.com/reaction/1654553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant4-(6-Hydroxyhexoxy)benzaldehydeHCID 15051082—
SolventWaterHCID 962—
Product4-(6-Acryloyloxyhexyloxy)benzaldehydeHCID 19602217—

Reaction Conditions

Temperature0 °C

Reaction Steps

8.9 g (0.04 mol) of 4-(6-hydroxyhexyloxy)benzaldehyde, 6.8 ml of triethylamine and 100 ml of acetonitrile were put in a three-neck flask equipped with a thermometer and a stirrer and cooled to 0° C. To this mixture was dropwise added a solution comprising 4.0 g (0.044 mol) of acryloyl chloride and 10 ml of acetonitrile with stirring at 0° C. to 5° C. After the addition, the whole mixture was stirred for one hour at 0° C. and poured into water containing ice. The crystals which precipitated out after a while were taken out by filtration, washed with water and dried by airing to obtain the intended compound. The yield of the product was 3.94 g (35.7%). The product had a melting point of 30° C. or lower.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05408009
Source datasetuspto-grants-1995_04
ORD IDord-c76380395ec44470a2b47e867b1373d6
Source noteuspto-grants-1995_04