HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659948Generated: October 27, 2026
4-Fluorobenzyl chloride → 4-[2-(4-Fluoro-phenyl)-1,1-dimethoxy-ethyl]-pyridine
https://huagongshe.com/reaction/659948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(Dimethoxymethyl)pyridine | HCID 642853 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-[2-(4-Fluoro-phenyl)-1,1-dimethoxy-ethyl]-pyridine | HCID 14956226 | 94.8% |
Reaction Steps
315 mL of n-butyllithium 1.6 M solution in hexane is added dropwise to a solution of 70.3 g (0.46 mole) of 4-dimethoxymethyl-pyridine in 1.4 L of tetrahydrofuran under nitrogen at −70° C. After 30 min. at −70° C., 73 g (0.505 mole) of 4-fluorobenzyl chloride in 280 mL of tetrahydrofuran is added dropwise. After 10 more min. at −70° C., the reaction mixture is allowed to reach room temperature and then stirred for 30 further min. The reaction mixture is poured into 2 L ammonium chloride solution and extracted with ethyl acetate. The organic phase is washed with water and dried over magnesium sulfate. After concentration the residue is purified by chromatography on silica gel (ethylacetate/hexane 1/1) to give 114 g of 4-[2-(4-Fluoro-phenyl)-1,1-dimethoxy-ethyl]-pyridine as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084395B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-5c983e7399a649d69d87e3adb06b90bd |
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| Source note | uspto-grants-2011_12 |
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