HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481755Generated: November 1, 2026
Triethylamine → Phosphonic acid, (4′-bromo[2,2′-bipyridin]-4-yl)-, diethyl ester
https://huagongshe.com/reaction/481755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethylphosphite | HCID 3780918 | — |
| Reactant | 4,4'-Dibromo-2,2'-bipyridine | HCID 15569987 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Phosphonic acid, (4′-bromo[2,2′-bipyridin]-4-yl)-, diethyl ester | HCID 54420157 | — |
Reaction Steps
2.0 g of 4,4'-dibromo-2,2-bipyridine (6.4 mmol), 0.9g of palladium tetrakistriphenylphosphine (0.8 mmol), 3.14 g of diethylphosphite (23 mmol) and 2.34 g of triethylamine (23 mmol) are measured into an argon filled 50 ml round bottom. flask, equipped with a cold finger (10 cm) and magnetic stirrer. This is heated on a 98° C. oil bath for 3 hours. The reaction is monitored with TLC on silica gel plates, DCM: MeOH (10:1), Rf-Lb=0.73. This is then cooled back to room temperature, and then the solidified mixture is added to 25 mls of methanol, stirred for 10 min. and evaporated to dryness under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05789592 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-86acc29aeb8a4fe7b2c0cda6adf90d5e |
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| Source note | uspto-grants-1998_08 |
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