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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329677Generated: October 25, 2026

Ethyl Acetate → potassium (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]-carbapen-2-em-3-carboxylate

https://huagongshe.com/reaction/329677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTriphenylphosphineHCID 11776—
Reactantallyl (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]carbapen-2-em-3-carboxylateHCID 14329067—
ReactantPotassium 2-ethylhexanoateHCID 23669619—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
SolventDichloromethane ethylacetateHCID 21226138—
Productpotassium (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]-carbapen-2-em-3-carboxylateHCID 131715759—

Reaction Steps

A solution of allyl (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]carbapen-2-em-3-carboxylate (42 mg, 0.15 mmol) and triphenylphosphine (12 mg, 0.045 mmol) in 1:1 methylene chloride-ethyl acetate (2.7 ml) is treated with 0.5M potassium 2-ethylhexanoate in ethyl acetate (0.3 ml, 0.15 mmol) and tetrakis(triphenylphosphine)palladium (O) (13.8 mg, 0.012 mmol). The mixture is stirred 15 minutes at ambient temperature under a nitrogen atmosphere, diluted with diethyl ether, and centrifuged. The insoluble pellet is washed with ether and dried under vacuum to afford potassium (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]-carbapen-2-em-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892869
Source datasetuspto-grants-1990_01
ORD IDord-1c4e9ced6a424a758fae9631ae9fc7db
Source noteuspto-grants-1990_01