HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255823Generated: October 26, 2026
Triphenylphosphine → (s)-1-(3-Nitrophenyl)ethanamine
https://huagongshe.com/reaction/1255823
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-[(1S)-1-azidoethyl]-3-nitrobenzene | HCID 86641855 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (s)-1-(3-Nitrophenyl)ethanamine | HCID 11292459 | 92% |
Reaction Steps
To a solution of 1-[(1S)-1-azidoethyl]-3-nitrobenzene (16.5 g, 86 mmol) in a mixture of toluene (325 mL) and water (40 mL) was added triphenylphosphine (44.5 g, 170 mmol) in one portion. The mixture was immediately heated to 80° C. where it was stirred for 3 hours. After this time the mixture was allowed to cool to room temperature, was diluted with ethyl acetate (100 mL), the two phases separated and the organic phase extracted with dilute aqueous hydrochloric acid (2M, 3×100 mL). The acidic extracts were basified to pH>10 with solid potassium hydroxide and were then extracted with dichloromethane (3×100 mL). The organic extracts were washed with brine (100 mL), dried (MgSO4) and concentrated under reduced pressure to give (1S)-1-(3-nitrophenyl)ethanamine (13.1 g, 92%) as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461161B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-f58733995c724d5f9552557869f9c78f |
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| Source note | uspto-grants-2013_06 |
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