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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540968Generated: October 29, 2026

Iodine → HCID 86672919, compound

https://huagongshe.com/reaction/540968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDimethylformamideHCID 6228—
ReactantMagnesiumHCID 5462224—
Reactant2-Bromo-3-(2-ethylhexyl)thiopheneHCID 58098291—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86672919HCID 8667291969%

Reaction Steps

To a mixture of magnesium turnings (0.61 g, 25.1 mmol), anhydrous THF (20 mL) and a small amount of iodine in a 300 mL flask, a solution of bromothiophene (9-5), (6.58 g, 23.9 mmol) in anhydrous THF (35 mL) was added slowly at 0° C. under N2. After refluxing for 1 h, the reaction mixture was transferred into a 250 mL flask at room temperature under N2. DMF (3.24 mL, 41.9 mmol) was added dropwise to the reaction mixture. After the mixture was stirred overnight at room temperature, the reaction was quenched by pouring cold HCl aq. (2 N) into the mixture. The product was extracted with CHCl3 and dried over anhydrous Mg2SO4. The crude product was further purified by column chromatography using hexane/CHCl3 (2:1) as the eluent to give (9-6) as a colourless oil (3.7 g, 69%). 1H NMR (CDCl3, 300 MHz, ppm): 10.03 (s, 1H), 7.64 (d, 1H, J=5.1 Hz), 6.98 (d, 1H, J=5.1 Hz), 2.89 (d, 2H, J=7.2 Hz), 1.56-1.64 (m, 1H), 1.27-1.37 (m, 8H), 0.86-0.91 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871884B2
Source datasetuspto-grants-2014_10
ORD IDord-50b6ed4d6d6b4c048a4ec27618b533f9
Source noteuspto-grants-2014_10