HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899985Generated: October 28, 2026
Triphenylphosphine dibromide → HCID 21874554, compound
https://huagongshe.com/reaction/899985
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine dibromide | HCID 70579 | — |
| Reactant | (2-Ethylpyridin-4-yl)methanol | HCID 9964106 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21874554 | HCID 21874554 | 14.2% |
Reaction Steps
A solution of 0.3 g of 2-ethyl-4-(hydroxymethyl)pyridine in 3.5 ml of dichloromethane is added dropwise to a solution of 1.25 g of dibromotriphenylphosphorane in 4 ml of dichloromethane, under an inert atmosphere of argon at a temperature in the region of 0° C. The mixture is stirred to a temperature in the region of 20° C. over about 1 hour. The reaction medium is taken up in 50 ml of dichloromethane and then washed with 3×50 ml of water. The organic phase is dried over magnesium sulfate, filtered and then concentrated to dryness under reduced pressure. The residue thus obtained is purified by flash chromatography using a cartridge 20 mm in diameter packed with 10 g of 20-40 μm conditioned silica, and then eluted with a mixture (cyclohexane/ethyl acetate) (9/1) (v/v), at a flow rate of 8 ml/minute. The fractions between 80 and 120 ml are concentrated under reduced pressure. 0.062 g of 2-ethyl-4-(bromomethyl)pyridine is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354933B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-fd7ecbc290be46c3beed9a3b35f7a673 |
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| Source note | uspto-grants-2008_04 |
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