HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625197Generated: October 30, 2026
1,4-Cyclohexanedione → HCID 66749276, compound
https://huagongshe.com/reaction/625197
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Cyclohexanedione | HCID 12511 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 77230807 | HCID 77230807 | — |
| Product | HCID 66749276 | HCID 66749276 | 87% |
Reaction Steps
5-Iodo-2,3-thiophenedicarboxaldehyde (20.00 g, 75.15 mmol) and 1,4-cyclohexandione (4.25 g, 37.12 mmol) were dissoved in IMS (industrial methylated spirits) (600 cm3) by warming and stirring, and then cooled to 20° C. with a water bath. 5% KOH solution (7.5 cm3) was added in one portion under nitrogen with vigorous stirring. The reaction mixture was stirred at 20° C. for 30 minutes and the precipitate formed was collected by suction filtration, washed with IMS, water, IMS, then acetone, and dried in the vacuum oven at 40° C. overnight to yield 2,8-diiodo-anthra[2,3-b:7,6-b′]dithiophene-5,11-dione (18.39 g, 87%). The solid was directly used for the following reactions without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09306172B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-9890c666390b494382866c53b301456e |
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| Source note | uspto-grants-2016_04 |
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