Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Octylamine | HCID 8143 | — |
| Reactant | HCID 57319167 | HCID 57319167 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 54513161 | HCID 54513161 | 69.1% |
Reaction Steps
A reactor was charged with 275 g (2.2 moles) of octylamine, and the contents were heated to 70° C. To the contents, a solution with 36 g (0.17 mole) of N,N-bis(3-chloro-2-hydroxypropyl)hydroxyethylamine dissolved in 30 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 500 ml of xylene and 500 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 50.7 g (yield: 69%) of 11,15-dihydroxy-13-hydroxyethyl-9,13,17-triazapentacosane represented by the following formula. ##STR13##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05801270 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-9d887df76e7a46ab95c4b2b5b1814d08 |
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| Source note | uspto-grants-1998_09 |
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