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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721085Generated: October 26, 2026

1-(Triphenylphosphoranylidene)acetone → 1-(N-Cbz-2-pyrrolidinyl)-1-buten-3-one

https://huagongshe.com/reaction/1721085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Triphenylphosphoranylidene)acetoneHCID 15038—
Reactant(S)-2-Formyl-pyrrolidine-1-carboxylic acid benzyl esterHCID 11746545—
SolventBenzeneHCID 241—
Product1-(N-Cbz-2-pyrrolidinyl)-1-buten-3-oneHCID 5727024669%

Reaction Steps

To a stirred solution of N-Cbz-L-prolinal (6.3 g, 27 mmol, from step 24d above) in 30 mL of benzene was added 9.42 g (29.6 mmol) of 1-triphenylphosphoranylidene-2-propanone (Aldrich) at room temperature. The reaction mixture was heated to reflux for 4 hr. The benzene was removed under vacuum, and the residue was dissolved in ether and cooled for 16 hr. The phosphine oxide by product was removed by filtration, and the solution was further purified by column chromatography on silica gel, eluting with 20% ethyl acetate in hexanes, to afford 4.4 g of the title product (69% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508418
Source datasetuspto-grants-1996_04
ORD IDord-ab2b654ca17c4d2885b3b030ae8eeda4
Source noteuspto-grants-1996_04