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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913550Generated: November 1, 2026

Triphenylphosphine → HCID 178471118, compound

https://huagongshe.com/reaction/1913550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantHCID 178418642HCID 178418642—
ReactantHCID 178471119HCID 178471119—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178471118HCID 17847111825.4%

Reaction Conditions

Temperature55 °C

Reaction Steps

The compound (170 mg) obtained in Step 2 of Example 37 was dissolved in tetrahydrofuran (6 mL). To the solution, triphenylphosphine (137 mg), 4-hydroxypyridine (50 mg), and a 40% solution of diisopropyl azodicarboxylate in toluene (276 μL) were added, and the mixture was stirred at 55° C. for 5.5 hours. The solvent in the reaction solution was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluting solvent: hexane/ethyl acetate=7/3-ethyl acetate) to obtain the title compound (51 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609710B2
Source datasetuspto-grants-2013_12
ORD IDord-d801cf95be2b4708b13e79454bafb0d8
Source noteuspto-grants-2013_12