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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1473913Erstellt: 23. Oktober 2026

Sodium borohydride → 3-Bromo-2-(hydroxymethyl)phenol

https://huagongshe.com/de/reaction/1473913

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt2-Bromo-6-hydroxybenzaldehydeHCID 11954768—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Bromo-2-(hydroxymethyl)phenolHCID 8612602560%

Reaktionsschritte

To a solution of 2-bromo-6-hydroxybenzaldehyde (3.8 g, 18.91 mmol, 1 eq.) in a mixture of THF and MeOH (4/1, 25 mL) was added NaBH4 (1.4 g, 37.81 mmol, 1.5 eq.) at rt portion-wise. Upon the completion of addition, the mixture was continued to stir at rt for 30 min. The mixture was quenched with HCl (4 N) and extracted with EtOAC twice. The combined organic layer was dried over Na2SO4, concentrated, and purified on silica gel using 25% EtOAc/hexanes as eluent to give 3-bromo-2-(hydroxymethyl)phenol (2.3 g, 60%) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09018210B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-b6a2b4f73fb24d26b0093fbe1e9f338d
Quellennotizuspto-grants-2015_04