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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367444Generated: October 26, 2026

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

https://huagongshe.com/reaction/1367444

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). 13C NMR: 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 numberUS07893191B2
Source datasetuspto-grants-2011_02
ORD IDord-283ec520e0f14bd79f5d02996f9212c4
Source noteuspto-grants-2011_02