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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905102Generated: October 31, 2026

Triphenylphosphine → HCID 131715980, compound

https://huagongshe.com/reaction/1905102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium 2-ethylhexanoateHCID 23672331—
ReactantHCID 131715979HCID 131715979—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 131715980HCID 13171598083%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04841042
Source datasetuspto-grants-1989_06
ORD IDord-016d7c3d05e8424a990cab2d15fc23c3
Source noteuspto-grants-1989_06