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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708604Generated: October 30, 2026

Triethylamine → HCID 86748205, compound

https://huagongshe.com/reaction/1708604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ReactantHCID 86748206HCID 86748206—
SolventDichloromethaneHCID 6344—
ProductHCID 86748205HCID 8674820544%

Reaction Steps

To a solution obtained by dissolving 211 mg of N-(4-hydroxyphenyl)-2-[(E)-1-(2,5-dimethyl-3-furyl)ethylidene]-3-isopropylidenesuccinimide obtained in Example 5 in 5 ml of dichloromethane, 72 mg of triethylamine was added, followed by dropwise addition of 66 mg of acryloyl chloride in 10 minutes. The reaction was carried out at room temperature for 30 minutes with stirring. After the reaction, the reaction solution was well washed with water, dried over anhydrous magnesium sulfate, and subjected to removal of the solvent by distillation. The resulting residue was purified by column chromatography (filler: Wakogel C-300, eluent: a mixed solvent of n-hexane and ethyl acetate) to give pale red crystals of N-(4-acryloyloxyphenyl)-2-[(E)-1-(2,5-dimethyl-3-furyl)ethylidene]-3-isopropylidenesuccinimide in yield of 44.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359085
Source datasetuspto-grants-1994_10
ORD IDord-ba6c23e6ace44815abd9520f8e4f93ef
Source noteuspto-grants-1994_10