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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76815Generated: October 29, 2026

HCID 58153059, compound → (2Z,3E,5Z)-5-(1,1-dioxido-3-oxo-1-benzothiophen-2(3H)-ylidene)-2-(1,3,3-trimethyl-1,3-dihydro-2H-indol-2-ylidene)pent-3-enenitrile

https://huagongshe.com/reaction/76815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58153059HCID 58153059—
ReactantHCID 67262655HCID 67262655—
Product(2Z,3E,5Z)-5-(1,1-dioxido-3-oxo-1-benzothiophen-2(3H)-ylidene)-2-(1,3,3-trimethyl-1,3-dihydro-2H-indol-2-ylidene)pent-3-enenitrileHCID 25156262—

Reaction Conditions

Temperature210 °C

Reaction Steps

A mixture of (1,3,3-trimethyl-2,3-dihydro-1H-indol-2-yl)acetonitrile (397 mg, 2.00 mmol) and (2Z)-2-[(2E)-3-methoxyprop-2-en-1-ylidene]-1-benzothiophen-3(2H)-one 1,1-dioxide (501 mg, 2.00 mmol) were placed in a 10-mL one-necked round bottom flask. The flask was heated in an oil bath at 210° C. for 2 hours and then cooled to room temperature. The reaction mixture was extracted with dichloromethane (100 mL). The organic solution was passed through a short silica column, the dichloromethane was evaporated and the pure dye was obtained by recrystallization from methanol. The yield was 511 mg of green crystals (63% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835632B2
Source datasetuspto-grants-2014_09
ORD IDord-a2b11419ae75457da89693b243276c18
Source noteuspto-grants-2014_09