HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 59497701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 59497358 | HCID 59497358 | — |
| Reactant | HCID 59497624 | HCID 59497624 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Aluminum | HCID 5359268 | — |
| Product | HCID 59497701 | HCID 59497701 | — |
Reaction Steps
To a stirred solution of the 3-(2-oxo-2,3-dihydro-benzimidazol-1-yl)-propionic acid methyl ester (100 mg, 0.45 mmol) and (2,3-Dimethyl-indolizin-8-yl)-methanol (88 mg, 0.50 mmol) in THF (8 ml) was added triphenylphosphine (143 mg, 0.54 mmol) followed by DIAD (0.11 ml, 0.54 mmol, dropwise) at ambient temperature. After five minutes the reaction became dark brown and was consequently wrapped in aluminum foil. After stirring over night the reaction was treated with silica gel and concentrated. The remaining solid was purified via column chromatography (silica gel, 5-40% EtOAc/hexanes). The product-containing fractions were combined and concentrated to give the product which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150556B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-302f2cec82584d83870362dc59a19ea3 |
| Source note | uspto-grants-2015_10 |