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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83967Generated: October 26, 2026

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

https://huagongshe.com/reaction/83967

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) is dissolved in DMF (100 mL). To this solution, N-bromosuccinimide (NBS) (4.78 g, 0.027 mol) in DMF (50 mL) is added dropwise in the dark and under argon. The resulting mixture is stirred at 0° C. for about three hours or until GC/MS shows a single peak at 415. This solution is poured into water (500 mL) and the organic solution is extracted with hexane (3×100 mL). The combined organic solutions are washed with brine (2×50 mL) and water (50 mL). After drying over MgSO4, the hexane is evaporated. The crude product is purified by column chromatography and eluted with hexane to yield the target compound (10.1 g, 90.2% yield). 1HNMR (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 numberUS08846855B2
Source datasetuspto-grants-2014_09
ORD IDord-5132c8694e44455ea30e4f6b7d9321b8
Source noteuspto-grants-2014_09