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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2274221Erstellt: 26. Oktober 2026

Borohydride → (2-Amino-5-bromo-3-fluorophenyl)methanol

https://huagongshe.com/reaction/2274221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBorohydrideHCID 28123—
Edukt2-Amino-5-bromo-3-fluorobenzoic acidHCID 40424597—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2-Amino-5-bromo-3-fluorophenyl)methanolHCID 5431252595%

Reaktionsschritte

To a solution of 2-amino-5-bromo-3-fluorobenzoic acid (14.5 g, 62.2 mmol) in THF (150 mL) at 0° C. was added borohydride in THF (1 M, 310 mL), and the reaction mixture was stirred at RT overnight. LCMS showed the reaction was completed. The reaction was quenched with methanol (150 mL), concentrated in vacuum, diluted with aqueous sodium bicarbonate (400 mL) and extracted with ethyl acetate (200 mL*3). The organic layers were separated, combined, washed with water (200 mL) and brine (200 mL), dried over sodium sulfate, filtered and concentrated to afford the title compound (13.0 g, crude), which was directly used in the next step without the further purification. MS (ES+) C7H7BrFNO requires: 219, 221. Found: 220, 222 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09126951B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-c17ee2bb848b45c7b8b2c3d53f3c7579
Quellennotizuspto-grants-2015_09