HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 10146789, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 1-(3,4,5-trimethoxy-benzoyl)-3-[2-[4-[1H-benzoimidazole-2-carbonyl]-piperidin-1-yl]-ethyl]-3-phenyl-pyrrolidine | HCID 10121390 | — |
| Reactant | 2-(3,3-Dimethylallyloxy)-ethanol | HCID 18333454 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | HCID 10146789 | HCID 10146789 | — |
Reaction Steps
Combine 1-(3,4,5-trimethoxy-benzoyl)-3-[2-[4-[1H-benzoimidazole-2-carbonyl]-piperidin-1-yl]-ethyl]-3-phenyl-pyrrolidine (0.62 g, 1.0 mmol), and 2-(3,3-dimethylallyloxy)-ethanol (0.14 g, 1.0 mmol), triphenylphosphine (0.33 g, 1.27 mmol) in tetrahydrofuran (2 mL). Add dropwise diethyl azodicarboxylate ((0.2 mL, 1.27.mmol). After 18 hours, evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 10% methanol/ethyl acetate to give the title compound: Rf=0.35 (silica gel, 10% methanol/ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329392B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-9b94b70539c9443f9eaba7de0ddb21f5 |
| Source note | uspto-grants-2001_12 |