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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21769Generated: October 26, 2026

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

https://huagongshe.com/reaction/21769

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 numberUS05424444
Source datasetuspto-grants-1995_06
ORD IDord-c84de9e588624ca4ad086efc5f1da219
Source noteuspto-grants-1995_06