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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 658072Erstellt: 25. Oktober 2026

3-Hydroxybenzaldehyde → 3-[(2,4,6-Trimethyl-benzylamino)-methyl]-phenol

https://huagongshe.com/reaction/658072

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-HydroxybenzaldehydeHCID 101—
EduktHydrochloric AcidHCID 313—
Edukt2,4,6-TrimethylbenzylamineHCID 458433—
EduktSodium BicarbonateHCID 516892—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
Produkt3-[(2,4,6-Trimethyl-benzylamino)-methyl]-phenolHCID 68982186—

Reaktionsschritte

3-Hydroxy-benzaldehyde (1.22 g, 0.01 mol) and 2,4,6-trimethyl-benzylamine (1.19 g, 0.01 mol) were added to methanol (10 mL) and the resulting mixture was stirred overnight. Sodium borohydride (0.45 g, 0.012 mol) was then added, and stirring was continued one hour. The resulting mixture was acidified with 2N HCl and then neutralized with saturated aqueous NaHCO3 solution to yield a gummy solution. The gummy solution was extracted with EtOAc (3×100 mL). The organic layer was washed with brine, dried over sodium sulfate, and concentrated in vacuo to yield a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08076358B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-be333cfe5a40457c91984a3e50d1a8c0
Quellennotizuspto-grants-2011_12