HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291752Generated: October 27, 2026
4-Nitrobenzaldehyde → 4-(1-Decenyl)nitrobenzene
https://huagongshe.com/reaction/1291752
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Decenyl)nitrobenzene | HCID 54217323 | — |
Reaction Steps
Phosphonium salt (141 g) obtained from n-nonyl bromide (115 ml) and triphenylphosphine (78.5 g) was dissolved in dry tetrahydrofuran (500 ml) and thereto was dropwise added n-butyl lithium (372 ml, 1.6M hexane solution) over not less than 1 hour at 0° C. After the dropwise addition, the reaction mixture was stirred at said temperature for 30 minutes and at room temperature for 1 hour. A solution of 4-nitrobenzaldehyde (45.3 g) in tetrahydrofuran (150 ml) was dropwise added thereto at 0° C. over 1 hour. The reaction mixture was stirred at room temperature for 10 hours and filtered. The residue was washed with ether. The filtrate was concentrated under reduced pressure and purified by silica gel column chromatography (hexane/ethyl acetate=100:1) to give 70.9 g of 4-(1-decenyl)-nitrobenzene (cis/trans=7:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753649 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-29be95ab18034f14b9542c25db9d9d82 |
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| Source note | uspto-grants-1998_05 |
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