HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899991Generated: October 30, 2026
Triphenylphosphine dibromide → HCID 59694328, compound
https://huagongshe.com/reaction/899991
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine dibromide | HCID 70579 | — |
| Reactant | HCID 11673394 | HCID 11673394 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59694328 | HCID 59694328 | 56.5% |
Reaction Steps
A solution of 0.5 g of 2,6-dibromo-4-(hydroxymethyl)pyridine in 7 ml of dichloromethane is added dropwise to a solution of 0.95 g of dibromotriphenylphosphorane in 5 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 2 hours. The reaction medium is taken up in 100 ml of dichloromethane and then washed with 100 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 37 mm in diameter packed with 50 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 135 and 200 ml are concentrated under reduced pressure. 0.349 g of 2,6-dibromo-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-3a76a31716b94dd4bcf6f11b95352ac4 |
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| Source note | uspto-grants-2008_04 |
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