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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2107366Erstellt: 25. Oktober 2026

Benzaldehyde → 2-Nitro-1-phenylbutan-1-ol

https://huagongshe.com/reaction/2107366

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktEthylenediaminetetraacetic AcidHCID 6049—
Edukt1-NitropropaneHCID 7903—
EduktButyllithiumHCID 178418339—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Nitro-1-phenylbutan-1-olHCID 22612361%

Reaktionsschritte

n-BuLi (1.6 M in hexane, 6.24 mL) was added dropwise with stirring to a solution of nitropropane (0.9 mL, 10 mmol) in THF (12 mL) at -78° C. After 15 minutes a solution of TiCl3 (OPriso) (5 mmol) in THF (2 mL) and CH2Cl2 (3 mL) solution was added. After a further 15 minutes benzaldehyde (0.5 mL, 5 mmol) was added and the mixture allowed to warm up to room temperature (~ 30 min.). Stirring was continued for a further 3.5 hours at room temperature and the mixture was quenched with an aqueous slurry of disodium EDTA (1.86 g, 5 mmol) and extracted with Et2O (3×75 mL). The combined Et2O fractions were washed with dilute hydrochloric acid (2 M, 75 mL), aqueous sodium bicarbonate (75 mL) and water (75 mL), dried and evaporated in vacuo. Flash column chromatography (SiO2 , hexane:Et2O, 6:1 v.v] gave 1-phenyl-2-nitro-butan-1-ol (0.57 g, 61%) erythro:threo ratio 6:1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04933505
Quelldatensatzuspto-grants-1990_06
ORD IDord-d5df211f5cf54063b248e2b7120c0891
Quellennotizuspto-grants-1990_06