HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116739Generated: October 26, 2026
Lauric Acid → 2,6-dimethyl-7a-undecyl-tetrahydro-2H-oxazolo[2,3-b]oxazole
https://huagongshe.com/reaction/2116739
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lauric Acid | HCID 3893 | — |
| Reactant | Diisopropanolamine | HCID 8086 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,6-dimethyl-7a-undecyl-tetrahydro-2H-oxazolo[2,3-b]oxazole | HCID 69203495 | — |
Reaction Steps
To a 5 liter stirred reactor, equipped with a distillation column, condenser, and graduated receiver, the following constituents were added: 1250.0 g of diisopropanol amine (DIPA) and 1502.5 g (98%) of lauric acid. The contents were heated to 186° C. under a nitrogen blanket over a 90 minute period. During that time, 136 ml of water came overhead. The batch temperature was held at 184° C. while the pressure was dropped to 320 Pa. During the pressure reduction, 410 g of unreacted DIPA came overhead. A total of 1192 g of amide acetal derived from lauric acid was collected while the temperature was raised to 220° C. at a pressure of 280-466 Pa. This represents a 53.5% conversion of the lauric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439354B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-00fb5ec26d9a42ca9d36a6a2cd4608c9 |
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| Source note | uspto-grants-2008_10 |
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