HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294730Generated: October 30, 2026
3-Nitrobenzaldehyde → HCID 58906331, compound
https://huagongshe.com/reaction/1294730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | N,N-diethyl-4-iodobenzamide | HCID 875218 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran toluene | HCID 22635083 | — |
| Product | HCID 58906331 | HCID 58906331 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07241764B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-a3238a19753546b68a7bae8c8a2490af |
|---|
| Source note | uspto-grants-2007_07 |
|---|