Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Chloroethanol | HCID 34 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Hexamethylene diisocyanate | HCID 13192 | — |
| Edukt | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| Edukt | Cardanol | HCID 11266523 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 131729245 | HCID 131729245 | 62% |
Reaktionsschritte
Cardanol was modified by coupling it with 2-chloroethanol in presence of K2CO3 and KI in DMF under inert atmosphere. Hexamethylene diisocyanate [HMDI] (0.49 g, 0.003 moles) in 10 ml dry DMF was taken in a 100 ml two necked flask and the contents were cooled with ice. HEMA (0.38 g, 0.003 moles) was added drop wise with constant stirring under nitrogen. The reaction was allowed to proceed under ice cold condition for 2 hr. Then the reaction was kept at room temperature for 1 hr. After that the reaction was changed to ice cold condition and 3 drops of DBTDL was added as catalyst followed by drop wise addition of modified cardanol (1 g, 0.003 moles) in 10 ml DMF. It was left stirring under cold condition for a further 1 hr and allowed to attain room temperature. Then the reaction was heated to 50° C. for 12 hrs. The contents were poured to 150 ml water and extracted with dichloromethane. It was then washed with plenty of water and dried in vacuum oven at 60° C. for 12 hrs. Yield=62% (1.17 g). The same synthetic procedure is adopted for all types of variation in the diisocyanate chemistry or in the hydroxy(meth)acryloxy chemistry or natural resource with active hydrogen atom to obtain the final UV curable telechelic pre polymer with varying R1, R2, R3, R4, R5 and R6.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08048979B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-40762ffc358245eabd6dd48c30a9c1a1 |
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| Quellennotiz | uspto-grants-2011_11 |
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