HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292555Generated: October 31, 2026
Dodecanoyl chloride → HCID 86752668, compound
https://huagongshe.com/reaction/1292555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dodecanoyl chloride | HCID 8166 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 15376645 | HCID 15376645 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86752668 | HCID 86752668 | 32.9% |
Reaction Steps
Bis(2-hydroxy-8-methyl-4,8-diazanonyl)ether (10 g, 0.030 mol) synthesized using a known method, triethylamine (6.1 g, 0.060 mol), and methylene chloride (200 ml) were placed in a 500 ml four-necked round flask, and the mixture was cooled on ice. Dodecanoylchloride (13 g, 0.060 mol) was added dropwise over 1 hour to the flask while the contents of the flask were stirred under nitrogen. The mixture was stirred for 24 more hours at room temperature. The solid which precipitated was removed by filtration, after which water was added for washing. Methylene chloride was removed from the organic phase under reduced pressure. The residue was purified by column chromatography (packed with Kieselgel 60 (product of Merck), eluent:chloroform/methanol=7:1 (v/v)) to obtain 6.9 g of bis(4-(1-oxododecyl)-2-hydroxy-8-methyl-4,8-diazanonyl)ether. Yield: 33 wt %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05756784 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-61f3a3a6ccc14dc8b18b485f6ad93a40 |
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| Source note | uspto-grants-1998_05 |
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