Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Octylamine | HCID 8143 | — |
| Reactant | HCID 18980722 | HCID 18980722 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 18980718 | HCID 18980718 | 83.3% |
Reaction Steps
A reactor was charged with 371 g (2.87 moles) of octylamine, and the contents were heated to 70° C. To the contents, a solution with 70 g (0.27 mole) of N,N-bis(3-chloro-2-hydroxypropyl)butylamine dissolved in 50 g of xylene was then added dropwise over 40 minutes. The resultant mixture was aged further for 4 hours. Thereafter, xylene was distilled off under reduced pressure, and unreacted octylamine was then distilled off at 70° C. and 0.5 mmHg. A mixture of 400 ml of xylene and 400 ml of 5% aqueous sodium hydroxide was added to the residue to subject it to extraction and washing. Thereafter, a xylene layer was taken out and concentrated, thereby obtaining 99.8 g (yield: 82%) of 11,15-dihydroxy-13-butyl-9,13,17-triazapentacosane represented by the following formula. ##STR11##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05929283 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-b8e9b4aaa99c468c8096249beed2b149 |
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| Source note | uspto-grants-1999_07 |
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