HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907247Generated: October 26, 2026
Water → 2-(2-(Bis(2-hydroxyethyl)amino)-2-oxoethyl)dec-3-enoic acid
https://huagongshe.com/reaction/907247
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diethanolamine | HCID 8113 | — |
| Reactant | 3-(1-Dodecen-1-yl)dihydro-2,5-furandione | HCID 32933 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2-(Bis(2-hydroxyethyl)amino)-2-oxoethyl)dec-3-enoic acid | HCID 72539810 | — |
Reaction Steps
A 500 ml, two-neck flask was charged with 52.6 g (500 mmol) diethanolamine and 50 ml toluene. A temperature probe was placed into this solution through one of the necks of the flask and the flask was immersed into a water bath. A solution of 105.2 g (500 mmol) dodecenylsuccinic anhydride dissolved in 200 ml toluene was dripped into the magnetically stirred solution diethanolamine solution over a 40-minute period. Ice was added to the water bath as required to prevent temperature of the reaction mixture from getting above 25° C. The mixture was then stirred for another 2.5 hours at room temperature. The complete disappearance of the anhydride functional group was confirmed by infrared spectroscopy. The FTIR trace on this compound had significant absorptions at 2957, 2924, 2858, 1733, 1616, 1560, 1415, 1160, 1069, 969, and 728 wavenumbers. The solution was concentrated down to 50% solids in toluene and was then set aside for later use.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08013104B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-81c3a10a6e46441dadd7ed913978c097 |
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| Source note | uspto-grants-2011_09 |
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