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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| Reactant | 1-Nitrohexane | HCID 12589 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Nitrophenyl)2-nitro-heptan-1-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04933505 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-7821a067a32a48798f43deb21c16d3d1 |
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| Source note | uspto-grants-1990_06 |
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