Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | 1-Dodecanol | HCID 8193 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Dodecyl glycidyl ether | HCID 17163 | 114.3% |
Reaction Steps
Dodecanol (167.4 g) and 8.1 g of trifluoromethanesulfonic acid were heated to 95° C. while stirring. To the reaction mixture, 166.5 g of epichlorohydrin was added dropwise over 1 hour, followed by stirring for 8 hours. After completion of the reaction, the reaction mixture was cooled to 50° C. Over 1 hour, 75 g of a 48% aqueous solution of sodium hydroxide was added dropwise at a temperature maintained at 50° C. After stirring for 3 hours, 120 mL of water was added to the reaction mixture to cause separation. The water layer thus occurred was removed. The residue was then washed twice with 100 mL of water, whereby 249 g of crude dodecyl glycidyl ether was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06437196B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-13ba51e981a2462ca60ca58669b50e59 |
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| Source note | uspto-grants-2002_08 |
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