HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52173Generated: October 29, 2026
Thiophene → 2-[(4-Fluorophenyl)methyl]thiophene
https://huagongshe.com/reaction/52173
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Fluorobenzyl bromide | HCID 68021 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(4-Fluorophenyl)methyl]thiophene | HCID 10583905 | 81% |
Reaction Steps
A solution of thiophene (12.6 g, 0.15 mol) in a mixture of anhydrous ether (230 mL) and anhydrous THF (70 mL) was treated dropwise at 0° C. with a 2.5M solution of n-butyllithium in hexane (54.0 mL, 0.134 mol). The mixture was stirred at 0° C. for 1.5 hours and then transferred by cannula into a -78° C. solution of 4-fluorobenzyl bromide (23.6 g, 0.125 mol) containing tetrakis(triphenylphosphine) palladium(0) (1.25 g) in anhydrous THF (200 mL). The reaction mixture was stirred at ambient temperature under nitrogen overnight and then quenched with saturated NH4Cl solution (100 mL) and partitioned between ether and additional NH4Cl solution. The ether layer was dried over MgSO4, concentrated in vacuo and the residue subjected to vacuum distillation to give 19.4 g (81% ) of 2-(4-fluorophenylmethyl)thiophene. b.p. 74°-83° C. at 0.6-0.7 mm of Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616596 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-c7035b63f308406b8daa8da500a0e393 |
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| Source note | uspto-grants-1997_04 |
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