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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitro-benzoic acid 1-hexyl-11-(4-nitro-phenoxy carbonyl)-undec-3-enyl esterHCID 131735514—
CatalystNickelHCID 935—
SolventEthyl AcetateHCID 8857—
ProductHCID 131735513HCID 131735513—

Reaction Conditions

Temperature62.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328192B2
Source datasetuspto-grants-2016_05
ORD IDord-82157e7f623d4c238fd369a736ff39f7
Source noteuspto-grants-2016_05