Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl Lactate | HCID 11040 | — |
| Edukt | Behenyl Alcohol | HCID 12620 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Produkt | Behenyl Lactate | HCID 54124846 | — |
Reaktionsschritte
Behenyl Lactate was prepared by reacting methyl lactate (Aldrich Chemical Company, Inc. of Milwaukee, Wis.) with Lanette 22 (behenyl alcohol, 90%, Henkel Corp. of Ambler, Pa.) in a transesterification reaction according to the following method: 0.2 g sodium hydride (60% in mineral oil) was added to 32.6 grams Lanette 22 at 70° C. in a 3-neck 250 ml glass flask purged with nitrogen and inserted with overhead stirrer, Dean Stark trap, thermometer, and condenser. To this was slowly added 9.4 g of methyl lactate and the contents were slowly heated to 160° C. and held at that temperature for one hour. At this temperature over 2 ml of methanol was collected. The contents were heated to 200° C. with a nitrogen sweep to remove any volatile components. After approximately 15 minutes at 200° C. the contents were cooled. Upon cooling the product crystallized and had a melting point of approximately 57° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06562360B2 |
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| Quelldatensatz | uspto-grants-2003_05 |
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| ORD ID | ord-4ded6f1664b6423b9bc2edee141afc71 |
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| Quellennotiz | uspto-grants-2003_05 |
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