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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1176215Erstellt: 27. Oktober 2026

Hydrochloric Acid → (4-Allyloxy-3-nitrophenyl)methanol

https://huagongshe.com/reaction/1176215

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium borohydrideHCID 4311764—
Edukt4-Allyloxy-3-nitrobenzaldehydeHCID 22401152—
LösungsmittelMethanolHCID 887—
Produkt(4-Allyloxy-3-nitrophenyl)methanolHCID 29006117—

Reaktionsschritte

The solution of 2.4 g of 4-allyloxy-3-nitrobenzaldehyde in 30 ml of methanol is cooled to 0° C. with stirring and subsequently admixed with 0.48 g of sodium borohydride in portions over 5 minutes. The reaction mixture is stirred further at 0° C. over 30 minutes, then poured onto cooled 2N HCl (100 ml) and extracted with tert-butyl methyl ether (2×100 ml). The organic phases are washed with water (100 ml), 1M sodium hydrogencarbonate solution (100 ml) and brine (100 ml), dried over sodium sulphate, filtered and concentrated by evaporation. The title compound is obtained as a slightly yellowish oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.12 (1:1 EtOAc-heptane); Rt=3.37.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07842688B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-a3947d4449d345dc8657db91218cb8d1
Quellennotizuspto-grants-2010_11