HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646538Generated: October 30, 2026
Tetrahydrofuran → 3-Bromo-4-hexylthiophene
https://huagongshe.com/reaction/646538
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,4,5-Tribromo-3-hexylthiophene | HCID 16103483 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Bromo-4-hexylthiophene | HCID 16103452 | 82.6% |
Reaction Steps
Compound 51 (70 g, 0.173 mol) was mixed with dry THF (400 mL). To this mixture, 7-butyllithium (138 mL, 2.5M in hexane, 0.345 mol) was added dropwise at −78° C. under argon. The resulting mixture was stirred for 10 minutes, then water (30 mL) was added to quench the reaction. The THF was evaporated and the organic was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with brine (2×100 mL), water (70 mL) and dried over MgSO4. After evaporation of the solvent, the resulting crude product was purified by vacuum distillation (72-74° C. at 0.17 mbar) to yield 52 (35.3 g, 82.6% yield). GC/MS: 246 g/mol (M-1). 1H NMR (CD2Cl2): δ 7.22 (s, 1H), 6.96 (s, 1H), 2.57 (t, 2H), 1.61 (m, 2H), 1.32 (m, 6H), 0.88 (t, 3H). 13C NMR: 141.92, 122.87, 120.95, 112.89, 31.88, 30.07, 29.53, 29.20, 22.88, 14.14.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07705108B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-44891ab122be413cb555162235fdb2ff |
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| Source note | uspto-grants-2010_04 |
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