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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107367Generated: October 25, 2026

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

https://huagongshe.com/reaction/2107367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantEthylenediaminetetraacetic AcidHCID 6049—
Reactant1-NitrohexaneHCID 12589—
ReactantButyllithiumHCID 178418339—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Nitrophenyl)2-nitro-heptan-1-olHCID 14817329—

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933505
Source datasetuspto-grants-1990_06
ORD IDord-7821a067a32a48798f43deb21c16d3d1
Source noteuspto-grants-1990_06