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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133801Generated: October 30, 2026

Triphenylphosphine → (1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethylazide

https://huagongshe.com/reaction/133801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(1R)-2-phenyl-1-(1,3-thiazol-2-yl)ethanolHCID 11084983—
SolventTetrahydrofuranHCID 8028—
Product(1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethylazideHCID 1095537482.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390910B2
Source datasetuspto-grants-2008_06
ORD IDord-b438dc3fffec42a9adf66b796ec4c0e2
Source noteuspto-grants-2008_06