HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Triphenylphosphoranylidene)acetone → HCID 67516599, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Triphenylphosphoranylidene)acetone | HCID 15038 | — |
| Reactant | HCID 86702733 | HCID 86702733 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 67516599 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09101133B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-92da134c1a4f4ba8acae772cbebb8e2c |
| Source note | uspto-grants-2015_08 |