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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485664Generated: October 30, 2026

Water → (S)-2-(2-amino-4-bromophenylamino)propan-1-ol

https://huagongshe.com/reaction/1485664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant(S)-2-(4-bromo-2-nitrophenylamino)propan-1-olHCID 118079386—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product(S)-2-(2-amino-4-bromophenylamino)propan-1-olHCID 9308157092.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

A 2-L, three-necked, round bottomed flask fitted with a nitrogen inlet, overhead stirrer, thermocouple, and condenser was charged with iron power (117 g, 2090 mmol), ammonium chloride (1.118 g, 20.90 mmol), ethanol (375 mL), and water (201 mL). The mixture was heated to 80° C., and a solution of (S)-2-(4-bromo-2-nitrophenylamino)propane-1-ol (57.5 g, 209 mmol) in ethanol (200 mL) was slowly added. The mixture stirred at 80° C. for 4 h. The reaction mixture was filtered through a pad of Celite and washed with ethanol (100 mL). The filtrate was concentrated under reduced pressure to remove the ethanol, and the resulting aqueous slurry stirred at rt for 3 h. The slurry was then filtered, and the solids were washed with water (100 mL) and dried under a nitrogen atmosphere overnight to afford (S)-2-(2-amino-4-bromophenylamino)propane-1-ol (47.55 g, 89%) as an off-white solid. MS (ESI, pos. ion) m/z 245 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422281B2
Source datasetuspto-grants-2016_08
ORD IDord-6f6089f00e734947b4c3c104e54fd1f2
Source noteuspto-grants-2016_08