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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625197Generated: October 30, 2026

1,4-Cyclohexanedione → HCID 66749276, compound

https://huagongshe.com/reaction/625197

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexanedioneHCID 12511—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 77230807HCID 77230807—
ProductHCID 66749276HCID 6674927687%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09306172B2
Source datasetuspto-grants-2016_04
ORD IDord-9890c666390b494382866c53b301456e
Source noteuspto-grants-2016_04