Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Acryloyl chloride | HCID 13140 | — |
| Edukt | 2-(2-Hydroxyethoxy)phenol | HCID 78519 | — |
| Katalysator | Phenothiazine | HCID 7108 | — |
| Produkt | 2-(Acryloyloxyethoxy)phenol acrylate | HCID 54320061 | 62% |
Reaktionsschritte
A 500-ml, two necked flask was equipped with magnetic stirring bar, nitrogen atmosphere and an addition funnel. The flask was charged with 25 g of 2-(2-hydroxyethoxy)phenol (0.16 mol.), 33 g of triethylamine (0.32 mol.), 250 ml of tetrahydrofuran and 1 g of phenothiazine. Next, 30 g of acryloyl chloride (0.18 mol.) was slowly added to the reaction over 1 hour via the addition funnel. The triethylamine hydrochloride salt was removed by filtration and the mother liquor was evaporated with a rotoevaporator. The remaining liquid was dissolved in chloroform and washed with NaCl(aq.), NH4OH(10%), NaCl(aq.) and dried over MgSO4. The chloroform was removed with a rotoevaporator to yield 26 g (62%) of a reddish brown liquid. The product was confirmed by IR and 13C NMR.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05523152 |
|---|
| Quelldatensatz | uspto-grants-1996_06 |
|---|
| ORD ID | ord-05328384b87746e0b7e8286a48450be6 |
|---|
| Quellennotiz | uspto-grants-1996_06 |
|---|