HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 54294615, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 4-(3,3-Dichloro-2-propenyloxy)-2,6-dichlorophenol | HCID 11346738 | — |
| Reactant | HCID 54435005 | HCID 54435005 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54294615 | HCID 54294615 | 67% |
Reaction Steps
To a mixture of 0.35 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenol, 0.32 g of 4-(hydroxymethyl)benzaldehyde O-(3,3-dichloro-2-propenyl)oxime, 0.32 g of triphenylphosphine, and 10 ml of dichloromethane was slowly added dropwise 0.25 g of diisopropyl azodicarboxylate. After stirring at room temperature for 12 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 0.43 g (yield, 67%) of 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyl)benzaldehyde O-(3,3-dichloro-2-propenyl)oxime, m.p., 76.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06437184B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-e7d29891610a484e8d370243bdf8d64d |
| Source note | uspto-grants-2002_08 |