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
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 58153059 | HCID 58153059 | — |
| Reactant | HCID 67262655 | HCID 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-enenitrile | HCID 25156262 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835632B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a2b11419ae75457da89693b243276c18 |
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| Source note | uspto-grants-2014_09 |
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