HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175100Generated: October 26, 2026
Water → 2-Bromo-3-decanyldithieno[3,2-b:2',3'-d]thiophene
https://huagongshe.com/reaction/1175100
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Decyldithieno[3,2-b:2',3'-d]thiophene | HCID 16103472 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromo-3-decanyldithieno[3,2-b:2',3'-d]thiophene | HCID 16103475 | 90.2% |
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%). 1H NMR: 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838623B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-4ad11e04b807438d9bc64507baf28337 |
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| Source note | uspto-grants-2010_11 |
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