HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 372918Erstellt: 24. Oktober 2026
1-Octanol → 1,8-Bis(octyloxymethyl)-3,6-dioxaoctane-1,8-diol
https://huagongshe.com/de/reaction/372918
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Octanol | HCID 957 | — |
| Edukt | Glycol diglycidyl ether | HCID 16683 | — |
| Edukt | Potassium | HCID 5462222 | — |
| Produkt | 1,8-Bis(octyloxymethyl)-3,6-dioxaoctane-1,8-diol | HCID 19812529 | 49% |
Reaktionsschritte
One part of ethylene glycol diglycidyl ether and 15 parts of octyl alcohol were reacted at 60° C. for 20 hours in the presence of 0.05 parts of potassium. Purification by distillation provided 1,8-bis(octyloxymethyl)-3,6-dioxaoctane-1,8-diol (boiling point 150° C./0.03 Torr) of the following formula: ##STR8## in a yield of 49%. This compound was then added to a greatly excess amount of a mixture of chlorosulfonic acid and acetic acid and reacted at room temperature for 3 hours. The resulting product was neutralized with sodium carbonate and extracted with n-butyl alcohol, obtaining a compound of the following formula: ##STR9## in a yield of 90%. This was a viscous liquid having a purity of 80% as measured by the modified Epton method which is a method for the quantitative measurement of anionic active agents.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05160450 |
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| Quelldatensatz | uspto-grants-1992_11 |
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| ORD ID | ord-d3c1242d532340d48582f45ccb784b9d |
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| Quellennotiz | uspto-grants-1992_11 |
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