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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469288Generated: October 26, 2026

Hydrochloric Acid → 2-(5-Methoxy-2-nitrophenyl)ethan-1-amine

https://huagongshe.com/reaction/469288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantBoraneHCID 6331—
Reactant(5-Methoxy-2-nitrophenyl)acetonitrileHCID 10867168—
SolventTetrahydrofuranHCID 8028—
Product2-(5-Methoxy-2-nitrophenyl)ethan-1-amineHCID 1862197577.4%

Reaction Steps

Under a nitrogen atmosphere 200 mL (200 mmol) of a 1M borane in THF solution were slowly added dropwise at RT to 12.6 g (65.7 mmol) (5-methoxy-2-nitrophenyl)-acetonitrile in 380 mL THF. The reaction mixture was refluxed for 2 h. After cooling, 30 mL methanol were added dropwise within 20 min. At the same time the temperature was maintained at 10° C. to 20° C. with an ice bath. The reaction mixture was stirred for 30 min at RT and then within 30 min 45 mL of a 2M HCl solution were added dropwise thereto. The reaction mixture was concentrated by rotary evaporation i. vac. with gentle heating. The residue was diluted to approx. 200 mL with water and extracted with 200 mL EtOAc. The aqueous phase was made alkaline with a 15% (w/v) aqueous potassium carbonate solution and continuously extracted with diethyl ether overnight using a rotary perforator according to Ludwig (Messrs Normag). The organic extract was concentrated to dryness by rotary evaporation. 9.98 g of the desired product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629137B2
Source datasetuspto-grants-2014_01
ORD IDord-908458147abb494caf1f3b27241a6771
Source noteuspto-grants-2014_01