HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865706Generated: October 31, 2026
Triphenylphosphine → (1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethylazide
https://huagongshe.com/reaction/1865706
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | (1R)-2-phenyl-1-(1,3-thiazol-2-yl)ethanol | HCID 11084983 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethylazide | HCID 10955374 | 82.7% |
Reaction Steps
Following the method of Itako et al. (Irako, N.; Hamada, Y.; Shioiri, T. Tetrahedron 48(35), 1992, 7251-7264), a solution of (1R)-2-phenyl-1-(1,3-thiazol-2-yl)ethanol (1.3 g, 6.3 mmol, from Reference Example 3) in tetrahydrofuran (60 mL) is cooled to 0° C. (ice-water bath). To the solution is added successively triphenylphosphine (1.8 g, 6.9 mmol), diethylazodicarboxylate (1.1 mL, 6.9 mmol), and diphenylphosphoryl azide (DPPA, 1.6 mL, 6.9 mmol). Following the addition of reagents, the reaction mixture is allowed to warm to room temperature and stir for 47 hours. Following this period, the mixture is concentrated under reduced pressure and purified by flash chromatography (silica gel, hexanes/toluene/diethyl ether) to give 1.2 g of (1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethylazide as a pale blond oil contaminated with DPPA (detected by 1H NMR).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07626023B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-f09f39ff0210452e8621cb6100f4780a |
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| Source note | uspto-grants-2009_12 |
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