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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2107367Erstellt: 24. Oktober 2026

4-Nitrobenzaldehyde → 1-(4-Nitrophenyl)2-nitro-heptan-1-ol

https://huagongshe.com/de/reaction/2107367

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-NitrobenzaldehydeHCID 541—
EduktEthylenediaminetetraacetic AcidHCID 6049—
Edukt1-NitrohexaneHCID 12589—
EduktButyllithiumHCID 178418339—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(4-Nitrophenyl)2-nitro-heptan-1-olHCID 14817329—

Reaktionsschritte

n-BuLi (1.6 M in hexane, 6.24 mL) was added dropwise with stirring to a solution of nitrohexane (1.4 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 4-nitrobenzaldehyde (0.75 mL, 5 mmol) in CH2Cl2 (3 mL) was added and the mixture allowed to warm up to room temperature (18 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), aqueous sodium bicarbonate (75 mL) and water (75 mL), dried and evaporated in vacuo. Flash column chromatography [SiO2, hexane:Et2O, 4:1 v/v] gave 1-(4-nitrophenyl)2 -nitro-heptan-1-ol (1.13 g, 81% Erythro:threo ratio 3.9:1

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04933505
Quelldatensatzuspto-grants-1990_06
ORD IDord-7821a067a32a48798f43deb21c16d3d1
Quellennotizuspto-grants-1990_06