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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 56448Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/56448

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBorohydrideHCID 28123—
Edukt2-Amino-5-bromo-3-chlorobenzoic acidHCID 827979—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2-Amino-5-bromo-3-chlorophenyl)methanolHCID 6708068482%

Reaktionsschritte

To a solution of 2-amino-5-bromo-3-chlorobenzoic acid (13.0 g, 52.0 mmol) in THF (200 mL) was added borohydride in THF (300 mL, 1N) at ice/water bath, and the reaction mixture was stirred at room temperature overnight. The mixture was quenched with methanol (100 mL) and concentrated to a volume of 50 mL. The residue was diluted with aqueous sodium bicarbonate (400 mL) and extracted with ethyl acetate (200 mL×3). The organic layers were separated, combined, washed by brine (100 mL), dried over sodium sulfate, filtered and concentrated to afford the title product (10.0 g, 82%). MS (ES+) C7H7BrClNO requires: 234, 236, found: 236, 238 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434700B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-2c837e710ae1411eb1a34020b955fe70
Quellennotizuspto-grants-2016_09