HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780546Generated: October 26, 2026
p-Bromophenyl octyl ether → HCID 178506738, compound
https://huagongshe.com/reaction/1780546
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromophenyl octyl ether | HCID 145298 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178506738 | HCID 178506738 | — |
Reaction Steps
31.38 g (110.0 mmol) of 1-bromo-4-octyloxybenzene in 80 ml of benzene and 81 ml (130.0 mmol) of a 1.6-molar n-butyllithium solution in hexane are stirred at room temperature under argon for 4 hours. The 4-octyloxyphenyllithium formed as a white precipitate is filtered off under argon, washed twice with 20 ml of n-hexane, dried in vacuo and slowly added dropwise as a solution in 60 ml of tetrahydrofuran at 0° C. under argon to a solution of 11.51 g (100.0 mmol) of 2,6-difluoropyridine in 80 ml of tetrahydrofuran. After a reaction time of 1 hour at 0° C., sodium chloride solution is added, the mixture is taken up in ether, the organic phase is washed with sodium chloride solution, dried over sodium sulfate, filtered, the solvent is removed from the filtrate, and the residue is purified by chromatography (silica gel, 9:1 hexane/ethyl acetate), giving 4.00 g of 2-fluoro-6-(4-octyloxyphenyl)pyridine. ##STR17##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05630962 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-e6d1a2fd748a44f1b1032e827b166bcf |
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| Source note | uspto-grants-1997_05 |
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