HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743333Generated: October 28, 2026
Triphenylphosphine → HCID 19423911, compound
https://huagongshe.com/reaction/743333
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(Dimethylamino)-1-propanol | HCID 76646 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 572468 | HCID 572468 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19423911 | HCID 19423911 | 36% |
Reaction Steps
134 mg of 3-(N,N-dimethylamino)propanol and 342 mg of triphenyl phosphine were added to a solution of 230 mg of 2-(3-phenylpropyl)phenol (prepared as described in Preparation 29) in 10 ml of methylene chloride, and the mixture was cooled with ice and stirred. 227 mg of diethyl azodicarboxylate were then added dropwise to the solution, and the mixture was stirred at room temperature for 5 hours. At the end of this time, the solvent was removed by distillation under reduced pressure, and ethyl acetate and water were added to the residue and shaken. The ethyl acetate layer was separated and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, using a 10:1 by volume mixture of methylene chloride and methanol as the eluent, to give 115 mg (yield 36%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05556864 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-0947e3ec2eea4ecdacb9bac1969f3a13 |
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| Source note | uspto-grants-1996_09 |
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