HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905102Generated: October 31, 2026
Triphenylphosphine → HCID 131715980, compound
https://huagongshe.com/reaction/1905102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium 2-ethylhexanoate | HCID 23672331 | — |
| Reactant | HCID 131715979 | HCID 131715979 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131715980 | HCID 131715980 | 83% |
Reaction Steps
2.8 ml (1.4 mmol - 1.05 equivalents) of 0.5 M sodium 2-ethylhexanoate in ethyl acetate, 35 mg (0.13 mmol - 0.1 equivalent) of triphenylphosphine and 35 mg (0.03 mmol) of tetrakis-(triphenylphosphine)-palladium (0) were successively added to a solution of 462 mg (1.33 mmol) of allyl (5R,6S)-2-(4-pyridylthio)-6-[(1R)-1-hydroxyethyl]-carbapen-2-em-3-carboxylate in 3.4 ml of anhydrous dichloromethane, and the mixture was stirred at room temperature for 1 h. It was then diluted with 20 ml of anhydrous acetone. The precipitate was filtered off with suction and vigorously stirred with 50 ml of ether for 0.5 h, again filtered off with suction and dried over P4O10 under high vacuum. 361 mg (83%) of the title compound were obtained as a colorless hygroscopic powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04841042 |
|---|
| Source dataset | uspto-grants-1989_06 |
|---|
| ORD ID | ord-016d7c3d05e8424a990cab2d15fc23c3 |
|---|
| Source note | uspto-grants-1989_06 |
|---|