HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088240Generated: November 2, 2026
Azobisisobutyronitrile → 11-(acryloylamino)undecanoic acid
https://huagongshe.com/reaction/2088240
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Methacrylate | HCID 87595 | — |
| Reactant | Ethylenedioxymethylamphetamine | HCID 24257269 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 11-(acryloylamino)undecanoic acid | HCID 235171 | — |
Reaction Steps
For the preparation of stationary phases, the inner walls of capillaries were vinylized with 3-(trimethoxylsilyppropyl methacrylate. Subsequently, AAUA, EDMA, 1-propanol, 1,4-butanediol, water, and AIBN were mixed ultrasonically into a homogenous solution and purged with nitrogen for 10 min. A 45 cm long silanized capillary was tilled with the polymerization mixture up to a length of 35 cm, sealed with rubber septum, and then placed in a gas chromatography (GC) oven to polymerize for 20 hours at 60° C. The reaction scheme for the polymerization is shown in Scheme 1. Each column of the experimental design was made in duplicate. After the polymerization of the mixture, the monolithic column was washed with methanol for 12 hours using a HPLC pump to remove unreacted monomers and porogens. An on-column detection window was made next to the polymer bed using a thermal wire stripper. Finally, the column was cut to 45 cm with an effective length of 30 cm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08435410B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-30bcf309d103495b8e0eac70c448f4d9 |
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| Source note | uspto-grants-2013_05 |
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