HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158120Generated: October 26, 2026
Glycerol → 2,3-Dihydroxypropyl 3-oxobutanoate
https://huagongshe.com/reaction/1158120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycerol | HCID 753 | — |
| Reactant | Lipoamide | HCID 863 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,3-Dihydroxypropyl 3-oxobutanoate | HCID 9898971 | — |
Reaction Steps
In accordance with at least one other embodiment of the present technology, glycerol can be treated with ethyl acetoacetate in presence of a lipase at from about 55° C. to about 70° C., alternatively from about 20 to about 75, for approximately 14 to 48 hours, alternatively 20 to 36 hours. The lipase can be, for example, Novozyme® 435, Lipozyme® RM IM, or Lipozyme® TL IM, all available from Novozymes A/S, Franklinton, N.C. The reaction can be performed in an inert (e.g., nitrogen) atmosphere. During the reaction, ethyl alcohol by-product can be removed, for example, via distillation. At the end of the reaction, the remaining ethyl acetoacetate can be removed through distillation (e.g., at 60° C., 1 mmHg). The structure of the triglyceride of acetoacetin produced can be confirmed through, for example, NMR analysis and/or GC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807718B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-51a29cc064194e87bb7a54163f2db38a |
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| Source note | uspto-grants-2010_10 |
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