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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255823Generated: October 26, 2026

Triphenylphosphine → (s)-1-(3-Nitrophenyl)ethanamine

https://huagongshe.com/reaction/1255823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-[(1S)-1-azidoethyl]-3-nitrobenzeneHCID 86641855—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(s)-1-(3-Nitrophenyl)ethanamineHCID 1129245992%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461161B2
Source datasetuspto-grants-2013_06
ORD IDord-f58733995c724d5f9552557869f9c78f
Source noteuspto-grants-2013_06