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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | (5-Methoxy-2-nitrophenyl)acetonitrile | HCID 10867168 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5-Methoxy-2-nitrophenyl)ethan-1-amine | HCID 18621975 | 77.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629137B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-908458147abb494caf1f3b27241a6771 |
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| Source note | uspto-grants-2014_01 |
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