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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742518Generated: October 27, 2026

Triethylamine → 4-((6-Acryloyloxy)hexyloxy)-4'-cyanobiphenyl

https://huagongshe.com/reaction/742518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant4'-(6-Hydroxyhexyloxy)-4-cyanobiphenylHCID 11173950—
SolventTetrahydrofuranHCID 8028—
Product4-((6-Acryloyloxy)hexyloxy)-4'-cyanobiphenylHCID 1141679570.8%

Reaction Steps

To a solution of 1.26 g (4.27 mmol) of the resulting compound (9) and 1.8 ml (24.8 mmol) of anhydrous triethylamine dissolved in 20 ml of tetrahydrofuran under argon atmosphere was added dropwise 5 ml of an tetrahydrofuran solution containing 0.38 ml (4.08 mmol) of acryloyl chloride. The whole was stirred at room temperature overnight, thereby a salt precipitated. After addition of water to the reaction mixture, the whole was extracted with diethyl ether. The extract was purified by silica gel column chromatography. The resulting pale yellow solid was recrystallized from methanol to obtain 1.01 g of 4-cyano-4'-(6-acryloxyhexyloxy)biphenyl (10) (yield: 67.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554706
Source datasetuspto-grants-1996_09
ORD IDord-007c31271c7848f7a18e4e8afd2e4329
Source noteuspto-grants-1996_09