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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646546Generated: October 26, 2026

Water → 2-Bromo-3-decanyldithieno[3,2-b:2',3'-d]thiophene

https://huagongshe.com/reaction/646546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Decyldithieno[3,2-b:2',3'-d]thiopheneHCID 16103472—
SolventDimethylformamideHCID 6228—
Product2-Bromo-3-decanyldithieno[3,2-b:2',3'-d]thiopheneHCID 1610347590.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-decanyldithieno[3,2-b:2′,3′-d]thiophene (91) (9.03 g, 0.027 mol) was dissolved in DMF (100 mL). To this solution, N-bromosuccinimide (NBS) (4.78 g, 0.027 mol) in DMF (50 mL) was added dropwise in the dark under argon. The resulting mixture was stirred at 0° C. for three hours. GC/MS showed a single peak at 415. This solution was poured into water (500 mL). Organic solution was extracted with hexane (3×100 mL). The combined organic solutions were washed with brine (2×50 mL) and water (50 mL). After drying over MgSO4, the hexane was evaporated. The crude product was purified by column chromatography and eluted with hexane to yield the target compound (10.1 g, 90.2%). 1HNMR: solvent, CD2Cl2. δ 7.39 (d, 1H), 7.29 (d, 1H), 2.74 (t, 2H), 1.74-1.33 (m, 16H), 0.89 (t, 3H). 13CNMR: 140.89, 140.63, 136.00, 131.55, 129.22, 126.58, 121.04, 108.89, 32.31, 29.94, 29.73 (overlap), 29.35, 28.49, 23.09, 14.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705108B2
Source datasetuspto-grants-2010_04
ORD IDord-6fbe095af2024cf1aad2087d3a46330a
Source noteuspto-grants-2010_04