HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746415Generated: October 31, 2026
Triphenylphosphine → HCID 86731591, compound
https://huagongshe.com/reaction/1746415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(Oxan-2-yloxy)ethan-1-ol | HCID 4166833 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 71543513 | HCID 71543513 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86731591 | HCID 86731591 | — |
Reaction Steps
An aliquot of tetrahydrofuran (THF) (1 mL) containing 4-((3,5-dimethylisoxazol-4-yl)methoxy)-N-(4-hydroxy-2-methylphenyl)-N-isobutylbenzenesulfonamide (50 mg, 0.112 mmol) and DIAD (0.048 mL, 0.247 mmol) was added to triphenylphosphine (64.9 mg, 0.247 mmol). The reaction mixture was sealed and left to stir for 10 minutes before addition of 2-((tetrahydro-2H-pyran-2-yl)oxy)ethanol (0.015 mL, 0.112 mmol). The sealed reaction mixture was then heated to 50° C. over night. LCMS showed the formation of the product. LCMS (M+1) 572, RT 1.4 mins. Used without further purification in next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150508B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-88c1f65f54fd4d2ea12cec2ffd854b88 |
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| Source note | uspto-grants-2015_10 |
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