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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133802Generated: October 29, 2026

Triphenylphosphine → (S)-2-phenyl-1-(thiazol-2-yl)ethanamine

https://huagongshe.com/reaction/133802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAmmonium HydroxideHCID 14923—
Reactant(1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethylazideHCID 10955374—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-phenyl-1-(thiazol-2-yl)ethanamineHCID 10198148—

Reaction Conditions

Temperature55 °C

Reaction Steps

To a 55° C. (oil bath) solution of triphenylphosphine (1.6 g, 6.3 mmol) in tetrahydrofuran (10 mL) is added (1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethylazide (contaminated with DPPA, 1.2 g, 5.2 mmol) as a solution in tetrahydrofuran (10 mL). The reaction mixture is allowed to stir for 2 hours at this temperature when aqueous ammonium hydroxide (14 mL) is added. Stirring at 55° C. is continued for 3 hours before the reaction mixture is stored in a −5° C. freezer overnight. The next morning, the reaction mixture is diluted with water (80 mL) and extracted twice with diethyl ether. The combined extracts are washed with 10% aqueous hydrochloric acid (70 mL). The acidic aqueous phase is cooled in an ice-water bath and then basified with 10% aqueous sodium hydroxide to pH 12. The basic phase is then extracted thrice with dichloromethane. The combined extracts are dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to provide a 0.67 g (52% over 2 steps) of a slightly blond oil. MS (ES+): (M+H)=205.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390910B2
Source datasetuspto-grants-2008_06
ORD IDord-22f592417bfc4f64b84936284a9a8312
Source noteuspto-grants-2008_06