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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253057Generated: October 31, 2026

Triphenylphosphine → HCID 66863232, compound

https://huagongshe.com/reaction/253057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-MorpholinoethanolHCID 61163—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantHCID 24828929HCID 24828929—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66863232HCID 66863232100%

Reaction Steps

To a solution of 1-(2-chlorophenyl)-5-(4-chlorophenyl)-3-ethoxycarbonyl-4-hydroxy-1H-pyrazole (200 mg, compound obtained in Reference Example 1 (4)) in tetrahydrofuran (4 mL) was added triphenylphosphine (208 mg) and 2-morpholino-ethanol (96 μL) and the mixture was stirred. Thereto was added dropwise diisopropyl azodicarboxylate (154 μL) at 0° C. under nitrogen-gas atmosphere and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo and the crude product was purified by column chromatography on silica gel (solvent: hexane/ethyl acetate=67/33 to 30/70) to obtain ethyl 1-(2-chlorophenyl)-5-(4-chlorophenyl)-3-ethoxycarbonyl-4-(2-morpholinoethoxy)-1H-pyrazole (463 mg, yield: 100%) as a colorless viscidity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872006B2
Source datasetuspto-grants-2011_01
ORD IDord-28bd15e72d1244309d6a7d84390d328b
Source noteuspto-grants-2011_01