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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85320Generated: October 25, 2026

Water → 2-[5-[2-(2-Benzyloxy-4-dibutylaminophenyl)vinyl]thiophene-2-yl]-3-cyano-2-butenedinitrile

https://huagongshe.com/reaction/85320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroformHCID 6212—
ReactantTetracyanoethyleneHCID 12635—
Reactant[3-Benzyloxy-4-[2-(thiophene-2-yl)vinyl]phenyl]dibutylamineHCID 68008929—
SolventDimethylformamideHCID 6228—
Product2-[5-[2-(2-Benzyloxy-4-dibutylaminophenyl)vinyl]thiophene-2-yl]-3-cyano-2-butenedinitrileHCID 8666760431.7%

Reaction Conditions

Temperature40 °C

Reaction Steps

In 3 ml of N,N-dimethylformamide, 0.13 g (1.01 mmol) of tetracyanoethylene was dissolved. With stirring under ice cooling, 0.4 g (0.95 mmol) of [3-benzyloxy-4-[2-(thiophene-2-yl)vinyl]phenyl]dibutyl amine was dissolved in 1 ml of N,N-dimethylformamide and added dropwise. The mixture was stirred for 40 minutes and further stirred with heating at 40° C. overnight. After the reaction mixture was poured into 100 ml of water, extraction with chloroform, washing with a saturated saline solution, drying over anhydrous sodium sulfate, and concentration were performed. The residue was purified by silica gel column chromatography and washed with ethanol to give 157 mg of a black crystal having a mp of 125-130° C. (yield: 31.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846955B2
Source datasetuspto-grants-2014_09
ORD IDord-77753e04cf7442b29f50ed8998c89950
Source noteuspto-grants-2014_09