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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107365Generated: October 29, 2026

4-Nitrobenzaldehyde → HCID 12808781, compound

https://huagongshe.com/reaction/2107365

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantEthylenediaminetetraacetic AcidHCID 6049—
Reactant1-NitropropaneHCID 7903—
ReactantButyllithiumHCID 178418339—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12808781HCID 1280878172%

Reaction Steps

n-BuLi (1.6 M in hexane, 6.24 mL) was added dropwise with stirring to a solution of nitropropane (0.9mL, 10mmol) 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 (4 mL) 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, 5mmol) 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 chromatrography [Si2, hexane:Et2O, 3:1 v/v] gave 1-(4-nitrophenyl)-2-nitro-butan-1-ol (0.86 g, 72%) Erythro:threo ratio 7:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933505
Source datasetuspto-grants-1990_06
ORD IDord-d0d5e09ac0394ddaa5c17b9144bf177e
Source noteuspto-grants-1990_06