Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708608Generated: October 29, 2026

Acryloyl chloride → HCID 18959639, compound

https://huagongshe.com/reaction/1708608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
ReactantHCID 18959648HCID 18959648—
SolventDichloromethaneHCID 6344—
ProductHCID 18959639HCID 1895963988.5%

Reaction Steps

To a solution obtained by dissolving 1.2 g of N-(4-hydroxyphenyl)-2-[(E)-1-(1,2-dimethyl-3-indolyl)ethylidene]-3-isopropylidenesuccinimide obtained in Example 16 in 25 ml of dichloromethane, followed by dropwise addition of 0.36 ml of acryloyl chloride in 10 minutes. The reaction was carried out at room temperature for additional 30 minutes with stirring. After the reaction, the reaction solution was well washed with water, dried over anhydrous magnesium sulfate, followed by 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 yellow crystals of N-(4-acryloyloxyphenyl)-2-[(E)-1-(1,2-dimethyl-3-indolyl)ethylidene]-3-isopropylidenesuccinimide in yield of 88.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359085
Source datasetuspto-grants-1994_10
ORD IDord-36282e40391f47dba915739335ea4ebd
Source noteuspto-grants-1994_10