HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522411Generated: October 31, 2026
Triphenylphosphine → HCID 89590639, compound
https://huagongshe.com/reaction/522411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 3-(Dimethylamino)-1-propanol | HCID 76646 | — |
| Reactant | HCID 178501303 | HCID 178501303 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89590639 | HCID 89590639 | 92% |
Reaction Steps
A reaction tube was charged with the product of step 5 (200 mg, 0.326 mmol) and triphenylphosphine (855 mg, 3.26 mmol). The tube was sealed and THF (3259 μl) was added via syringe at 0° C. 3-dimethylamino-1-propanol (381 μl, 3.26 mmol) was added followed by slow addition of diisopropyl azodicarboxylate (631 μl, 3.26 mmol). After 5 minutes 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. for 3 hours. The reaction mixture was concentrated to dryness in rotavap and the residue was purified on a gold cap silica gel (80 g) column (gradient: 0 to 60% solvent B in dichloromethane (solvent B: 20% methanol in ethyl acetate)) to give the title compound (210 mg, 0.300 mmol, 92% 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-9197bf62ecf4459390d1e6ff4831e64c |
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| Source note | uspto-grants-2016_05 |
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