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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335355Generated: October 28, 2026

Tetradodecyl benzo[1,2-b:4,5-b']dithiophene-4,4,8,8-tetracarboxylate → Didodecyl benzo[1,2-b:4,5-b']dithiophene-4,8-dicarboxylate

https://huagongshe.com/reaction/335355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetradodecyl benzo[1,2-b:4,5-b']dithiophene-4,4,8,8-tetracarboxylateHCID 86711081—
SolventDimethylformamideHCID 6228—
ProductDidodecyl benzo[1,2-b:4,5-b']dithiophene-4,8-dicarboxylateHCID 7098371732.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a one-necked flask, tetradodecyl benzo[1,2-b:4,5-b′]dithiophene-4,4,8,8-tetracarboxylate (9.0 g, 8.65 mmol) was dispersed in DMF (80 mL). The mixture was stirred at 120° C. for 10 minutes until the solution became clear. After air was purged in the flask, NaI (800 mg) was added and the reaction mixture was refluxed for 24 hours. After the solvent was evaporated under vacuum, water (30 mL) was added to the residue to form a mixture, which was extracted with CH2Cl2. The organic layer was combined, dried, and concentrated. The crude product was purified by flash chromatography (eluent: CH2Cl2:hexane=7:3) to give didodecyl benzo[1,2-b:4,5-b′]dithiophene-4,8-dicarboxylate (yield: 1.75 g, 32.9%). 1H NMR (CDCl3): 0.9 (6H, t), 1.3 (28H, m), 1.4 (4H, m), 1.6 (4H, m), 1.9 (4H, m), 4.6 (4H, t), 7.8 (2H, d), 8.3 (2H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883954B2
Source datasetuspto-grants-2014_11
ORD IDord-d3afdc33ba9d4c98981212f2b6a3c6d2
Source noteuspto-grants-2014_11