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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294730Generated: October 30, 2026

3-Nitrobenzaldehyde → HCID 58906331, compound

https://huagongshe.com/reaction/1294730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantAmmonium ChlorideHCID 25517—
ReactantN,N-diethyl-4-iodobenzamideHCID 875218—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventTetrahydrofuran tolueneHCID 22635083—
ProductHCID 58906331HCID 5890633150%

Reaction Conditions

Temperature-78 °C

Reaction Steps

N,N-Diethyl-4-iodobenzamide (5.0 g, 16 mmol) was dissolved in THF (150 mL) and cooled to −78° C. under nitrogen atmosphere. n-BuLi (15 mL, 1.07 M solution in hexane, 16 mmol) was added dropwise during 10 min at −65 to −78° C. The solution was then canulated into 3-nitrobenzaldehyde (2.4 g, 16 mmol) in toluene/THF (approx. 1:1, 100 mL) at −78° C. NH4Cl (aq.) was added after 30 min. After concentration in vacuo, extraction with EtOAc/water, drying (MgSO4) and evaporation of the organic phase, the residue was purified by chromatography on silica (0-75% EtOAc/heptane) to give INTERMEDIATE 2 (2.6 g, 50%). 1H NMR (CDCl3) δ 1.0-1.3 (m, 6H), 3.2, 3.5 (2m, 4H), 5.90 (s, 1H), 7.30-7.40 (m, 4H), 7.50 (m, 1H), 7.70 (d, J=8 Hz, 1H), 8.12 (m, 1H), 8.28 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241764B2
Source datasetuspto-grants-2007_07
ORD IDord-a3238a19753546b68a7bae8c8a2490af
Source noteuspto-grants-2007_07