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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646538Generated: October 30, 2026

Tetrahydrofuran → 3-Bromo-4-hexylthiophene

https://huagongshe.com/reaction/646538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2,4,5-Tribromo-3-hexylthiopheneHCID 16103483—
SolventWaterHCID 962—
Product3-Bromo-4-hexylthiopheneHCID 1610345282.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705108B2
Source datasetuspto-grants-2010_04
ORD IDord-44891ab122be413cb555162235fdb2ff
Source noteuspto-grants-2010_04