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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511747Generated: October 31, 2026

1-(Triphenylphosphoranylidene)acetone → HCID 67516599, compound

https://huagongshe.com/reaction/511747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Triphenylphosphoranylidene)acetoneHCID 15038—
ReactantHCID 86702733HCID 86702733—
SolventChloroformHCID 6212—
ProductHCID 67516599HCID 67516599—

Reaction Steps

1.87 g (4.65 mmol) of 6-(benzyloxy)-5-(2,6-diethyl-4-methylphenyl)-4-oxo-1,2,3,3a,4,6a-hexahydropentalene-2-carbaldehyde (compound I-a-2) and 1.63 g (5.11 mmol) of acetonylidenetriphenylphosphorane in 40 ml of trichloromethane are stirred at room temperature for 12 h. The solvent is then removed, and the residue is purified chromatographically on silica gel (mobile phase ethyl acetate/hexane 1:5). This gives 1.37 g (66%) of 3-benzyloxy-2-(2,6-diethyl-4-methylphenyl)-5-(3-oxobut-1-enyl)-4,5,6,6a-tetrahydro-3aH-pentalen-1-one as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09101133B2
Source datasetuspto-grants-2015_08
ORD IDord-92da134c1a4f4ba8acae772cbebb8e2c
Source noteuspto-grants-2015_08