HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282457Generated: October 26, 2026
Tetrahydrofuran → 1,1-Bis(4-dimethylaminophenyl)-2-(diphenylphosphino)propene
https://huagongshe.com/reaction/1282457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Chlorodiphenylphosphine | HCID 66180 | — |
| Reactant | 1,1-Bis(4-dimethylaminophenyl)-2-bromopropene | HCID 18424498 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,1-Bis(4-dimethylaminophenyl)-2-(diphenylphosphino)propene | HCID 12010826 | 68.2% |
Reaction Steps
Into a reactor were introduced 3.0 g (8.3 mmol) of the 1,1-bis(4-dimethylaminophenyl)-2-bromopropene and 10 mL of THF under a nitrogen atmosphere. The contents were cooled to −60° C. Thereto was gradually added dropwise 5.2 mL (8.3 mmol; 1.6 M hexane solution) of butyllithium. The resultant mixture was stirred for 30 minutes. Thereafter, 1.1 mL (6.0 mmol) of chlorodiphenylphosphine was added thereto and this mixture was heated to room temperature and stirred for 16 hours. Water was added to the reaction mixture. The resultant mixture was extracted with ethyl acetate, and the extract was dried with anhydrous magnesium sulfate. Thereafter, the solvent was removed under reduced pressure. The concentrate was recrystallized twice from hexane/ethanol to obtain 1.9 g (60%) of the target compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455720B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-807e04636f8e4173995de69f9ad973c4 |
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| Source note | uspto-grants-2002_09 |
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