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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305055Generated: November 2, 2026

Triphenylphosphine → HCID 18429639, compound

https://huagongshe.com/reaction/2305055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant4-(Hydroxymethyl)benzaldehydeHCID 556330—
Reactant4-(3,3-Dichloro-2-propenyloxy)-2,6-dichlorophenolHCID 11346738—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18429639HCID 1842963946.8%

Reaction Steps

To a mixture of 3.40 g of p-(hydroxymethyl)benzaldehyde obtained in the same manner as described above, 7.2 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 6.56 g of triphenylphosphine, and 50 ml of tetrahydrofuran was slowly added dropwise 5.05 g of diisopropyl azodicarboxylate with stirring under ice cooling. 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 4.75 g (yield, 46%) of 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyl)benzaldehyde, m.p., 93.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437184B1
Source datasetuspto-grants-2002_08
ORD IDord-58c279f28f05495b828ba3f903f194d7
Source noteuspto-grants-2002_08