HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522191Generated: October 28, 2026
4-Nitro-benzoic acid 1-hexyl-11-(4-nitro-phenoxy carbonyl)-undec-3-enyl ester → HCID 131735513, compound
https://huagongshe.com/reaction/522191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitro-benzoic acid 1-hexyl-11-(4-nitro-phenoxy carbonyl)-undec-3-enyl ester | HCID 131735514 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131735513 | HCID 131735513 | — |
Reaction Steps
To a solution of 4-nitro-benzoic acid 1-hexyl-11-(4-nitro-phenoxy carbonyl)-undec-3-enyl ester (300 g) in ethyl acetate (1.5 L) in a pressure vessel was added Raney Nickel (120 g) added, and the mixture stirred under an atmosphere of Hydrogen (8-10 Kg) for 8 hours at a temperature of 60-65° C. The catalyst was removed by filtration. The solvent was distilled off completely under reduced pressure at 65-70° C. and removed traces for 1 hour at 85-90° C. to get pure 4-aminobenzoic acid 11-(4-amino-phenoxycarbonyl)-1-hexyl-undec-3-enyl ester product as deep yellow thick syrup (190 g). The resulting compound was characterized by 1H NMR (CDCl3) δ 0.88 (t, 3H, CH3), 1.2-1.65 (m, 24H, 12×CH2), 2.12 (t, 2H, COCH2), 3.5 (m, 1H, CH) 5.12 (m, 1H, CH), 5.45 (m, 1H, CH), 6.55 (m, 4H, Ar), 6.85 (m, 2H, Ar), 7.75 (m, 2H, Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328192B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-82157e7f623d4c238fd369a736ff39f7 |
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| Source note | uspto-grants-2016_05 |
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