HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030028Generated: October 26, 2026
p-Bromophenyl octyl ether → 2-[4-(Octyloxy)-phenyl]-5-[(tetrahydro-2-pyranyloxy)methyl]pyridine
https://huagongshe.com/reaction/1030028
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromophenyl octyl ether | HCID 145298 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Chloro-5-{[(oxan-2-yl)oxy]methyl}pyridine | HCID 22127378 | — |
| Catalyst | Diphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chloride | HCID 21654969 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[4-(Octyloxy)-phenyl]-5-[(tetrahydro-2-pyranyloxy)methyl]pyridine | HCID 19821245 | 67.2% |
Reaction Steps
A Grignard reagent solution prepared from 0.8 g of magnesium, 10.3 g of (4-bromophenyl) octyl ether and 50 ml of tetrahydrofuran was added dropwise at 0°-5° C. within 30 minutes to a mixture of 7.5 g of crude 2-chloro-5-[(tetrahydro-2-pyranyloxy)methyl]pyridine, 75 ml of tetrahydrofuran and 0.36 g of 1,3-bis(diphenylphosphino)-propanenickel-(II) chloride. The reaction mixture was stirred for 3 hours, left to stand overnight, then adjusted to pH 8 with aqueous sodium hydrogen carbonate solution and diluted with diethyl ether. The organic phase was washed neutral with water, dried over sodium sulfate and concentrated. Chromatographic purification of the residue (14.6 g) on 210 g of silica gel with hexane/ethyl acetate (vol. 4:1) yielded 8.8 g of 2-[4-(octyloxy)-phenyl]-5-[(tetrahydro-2-pyranyloxy)methyl]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05104569 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-353edb4686bd4b7699d7958b0d957b13 |
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| Source note | uspto-grants-1992_04 |
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