HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41836Generated: October 29, 2026
Azobisisobutyronitrile → Sodium 3,4-bis[(2-ethylhexyl)oxycarbonyl]cyclohexanesulfonate
https://huagongshe.com/reaction/41836
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 1,2-Bis(2-ethylhexyl) 4-cyclohexene-1,2-dicarboxylate | HCID 520413 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Sodium 3,4-bis[(2-ethylhexyl)oxycarbonyl]cyclohexanesulfonate | HCID 86670194 | — |
Reaction Steps
In the stream of an argon gas, 80 g of 4-cyclohexene-1,2-dicarboxylic di(2-ethylhexyl)ester (manufactured by Tokyo Chemical Industry Co., Ltd.) and 900 mL of isopropyl alcohol was placed. 660 mL of an aqueous solution of 42.3 g of sodium hydrogen sulfite (manufactured by Wako Pure Chemical Industries, Ltd.) was added. The resulting solution was heated to a reflux temperature, and stirred at 80 to 83° C. for 16 hours. During this stirring, every one hour from the start to 1 to 5 hours after the start of refluxing, as well as after 9 hours and 10 hours, 1.66 g of 2,2′-azobis(isobutyronitrile) (manufactured by Wako Pure Chemical Ltd.) was added. After cooling to room temperature, the reaction liquid was concentrated under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08535812B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-43f62bcafd254a00bdc53b94ba711a8f |
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| Source note | uspto-grants-2013_09 |
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