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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 564495Erstellt: 24. Oktober 2026

Hydrochloric Acid → (3-Bromo-4-methoxyphenyl)methanamine

https://huagongshe.com/de/reaction/564495

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBoraneHCID 6331—
EduktTetrahydrofuranHCID 8028—
Edukt3-Bromo-4-methoxybenzonitrileHCID 736049—
LösungsmittelEthanolHCID 702—
Produkt(3-Bromo-4-methoxyphenyl)methanamineHCID 22026276—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

3-Bromo-4-(methyloxy)benzonitrile (2.12 g, 10 mmol), THF (30 mL), and 1.5 M borane in THF (30 mL, 45 mmols) were combined and stirred under argon at reflux. The additional 1.5 M borane in THF (30 mL, 45 mmols) and reflux continued. THF (30 mL), and 1.5 M borane in THF (30 mL, 45 mmols) was again added and the mixture refluxed for a total of ten days to drive the reaction to completion. The reaction was worked up by the cautious addition of ethanol followed by 1N HCl until the pH was 2. This mixture was then heated to 50° C. for 4 h. The solvents were pumped off, and the residue partitioned between EtOAc and water. The aqueous phase was washed 3× with EtOAc and adjusted to pH 10 by the addition of 2.5 N NaOH. The aqueous phase was extracted 3× with EtOAc. The combined organic phases were dried over anhydrous Na2SO4, filtered and concentrated to give the title compound. LC-MS m/z 198.7 (M−NH2), 0.99 min (ret time).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08067408B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-49cc177301fa4a26926a7c90e5ac8efe
Quellennotizuspto-grants-2011_11