HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253057Generated: October 31, 2026
Triphenylphosphine → HCID 66863232, compound
https://huagongshe.com/reaction/253057
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | HCID 24828929 | HCID 24828929 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66863232 | HCID 66863232 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872006B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-28bd15e72d1244309d6a7d84390d328b |
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| Source note | uspto-grants-2011_01 |
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