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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | (1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethylazide | HCID 10955374 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-phenyl-1-(thiazol-2-yl)ethanamine | HCID 10198148 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07390910B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-22f592417bfc4f64b84936284a9a8312 |
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| Source note | uspto-grants-2008_06 |
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