HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522408Generated: October 30, 2026
Triphenylphosphine → HCID 89590849, compound
https://huagongshe.com/reaction/522408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Piperidinol, 1-methyl- | HCID 66048 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | HCID 178501304 | HCID 178501304 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89590849 | HCID 89590849 | 97% |
Reaction Steps
A reaction tube was charged with the product of step 5 (400 mg, 0.674 mmol) and triphenylphosphine (1414 mg, 5.39 mmol). The tube was sealed and THF (6737 μl) was added via syringe at 0° C. 4-hydroxy-1-methylpiperidine (633 μl, 5.39 mmol) was added followed by slow addition of diisopropyl azodicarboxylate (1044 μl, 5.39 mmol). After 5 min, the cooling bath was removed and the mixture was allowed to reach room temperature and stirred for 10 minutes. The reaction tube was heated at 40° C. LCMS showed complete reaction after 2 hours. The reaction mixture was concentrated to dryness in rotavap and the residue was purified on a gold cap silica gel (120 g) column (gradient: 0 to 50% solvent B in dichloromethane (solvent B: 20% methanol in ethyl acetate)) to give the title compound (450 mg, 0.651 mmol, 97% yield) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328138B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-f2bc9b4e299e4b31b0029332e51056d9 |
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| Source note | uspto-grants-2016_05 |
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