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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650320Generated: October 30, 2026

Morpholine → 2-Methylhept-2-enoic acid

https://huagongshe.com/reaction/1650320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriphenylphosphineHCID 11776—
Reactantallyl (5R,6S)-3-[2-{(2S)-1-allyloxycarbonyl-4-fluoropyrrolidin-2-yl}-1-methylethenyl]-6-[(1R)-1-hydroxyethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylateHCID 86743911—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product2-Methylhept-2-enoic acidHCID 53411097—

Reaction Steps

To a solution of allyl (5R,6S)-3-[2-{(2S)-1-allyloxycarbonyl-4-fluoropyrrolidin-2-yl}-1-methylethenyl]-6-[(1R)-1-hydroxyethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (1.7 g), morpholine (694 μl), and triphenylphosphine (199 mg) in tetrahydrofuran (30 ml) and ethanol (10 ml) was added tetrakis(triphenylphosphine)palladium(0) (263 mg) at room temperature. After stirring for an hour, the precipitate was filtered, washed in turn with dichloromethane (3 times) and acetone (twice), and dried under reduced pressure to give (5R,6S)-3-[2-{(2S)-4-fluoropyrrolidin-2-yl}-1-methylethenyl]-6-[(1R)-1hydroxyethyl]-7-oxo-1-azabicyclo 3.2.0]hept-2-ene-2carboxylic acid (248 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923857
Source datasetuspto-grants-1990_05
ORD IDord-7e4eaef3f42d41b68ddd38ec7d77cf53
Source noteuspto-grants-1990_05