HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486497Generated: October 26, 2026
Phosphanium bromide → HCID 178438821, compound
https://huagongshe.com/reaction/486497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphanium bromide | HCID 21868956 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178441846 | HCID 178441846 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178438821 | HCID 178438821 | — |
Reaction Steps
To a suspension of 3.66 g of methyltriphenylphosphonium bromide in 30 ml of dry tetrahydrofuran, cooled to -78° C., is added dropwise 5.9 ml of a 1.73M solution of n-butyllithium in hexanes. Following complete addition, the reaction mixture is allowed to warm to room temperature and stirred for 15 minutes, until all the phosphonium bromide is dissolved. The reaction mixture is then recooled to -78° C. and a suspension of 6-acetyl-2-butyl-4(1H)-quinazolinone in 15 ml of dry tetrahydrofuran is added. The reaction is allowed to warm to room temperature and stirred for 24 hours followed by quenching with saturated ammonium chloride solution. After diluting with 10 ml of water, the aqueous layer is extracted with chloroform and the combined organics dried over magnesium sulfate, filtered and concentrated in vacuo. The residue is purified by flash chromatography on silica gel, eluting with 1:2 ethyl acetate-hexanes to give 0.23 g of the desired product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292734 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-8ed55d49f666477ba4dae468563bd85b |
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| Source note | uspto-grants-1994_03 |
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