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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872307Generated: October 25, 2026

Triethylamine → 2-methoxy-4-[(E)-2-methoxycarbonyl-vinyl]-phenyl 4-[6-(2-methyl-acryloyloxy)-hexyloxy]-benzoate

https://huagongshe.com/reaction/1872307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 4-hydroxy-3-methoxy-cinnamateHCID 16830—
ReactantThionyl ChlorideHCID 24386—
Reactant4-[6-(2-Methyl-acryloyloxy)-hexyloxy]-benzoateHCID 7021645—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-methoxy-4-[(E)-2-methoxycarbonyl-vinyl]-phenyl 4-[6-(2-methyl-acryloyloxy)-hexyloxy]-benzoateHCID 1832918350.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

8.5 g (0.028 mol) of 4-[6-(2-methyl-acryloyloxy)-hexyloxy]-benzoate were treated with 6 ml of thionyl chloride and 3 drops of DMF and the mixture was heated to 90° C. for 2 hours. The excess thionyl chloride was completely removed firstly in a water-jet vacuum and subsequently in a high vacuum. The residual acid chloride was taken up in 20 ml of dichloromethane and slowly added dropwise at 0° C. to a solution of 5.25 g (0.025 mol) of methyl 4-hydroxy-3-methoxy-cinnamate and 4.25 ml of triethylamine in 25 ml of THF. The batch was stirred at room temperature overnight, filtered and the filtrate was evaporated to dryness. The residue was purified by column chromatography on silica gel with dichloromethane/diethyl ether (19:1) and subsequently by recrystallization from ethanol/THF. 6.31 g of 2-methoxy-4-[(E)-2-methoxycarbonyl-vinyl]-phenyl 4-[6-(2-methyl-acryloyloxy)-hexyloxy]-benzoate were isolated as a white powder; m.p. 92-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107427
Source datasetuspto-grants-2000_08
ORD IDord-62f38aa2bfe545c8b5dd6142fcea5a7e
Source noteuspto-grants-2000_08