Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triisopropyl phosphite | HCID 8304 | — |
| Edukt | Acetic acid 2-chloromethoxy-ethyl ester | HCID 10034810 | — |
| Produkt | Diisopropyl phosphite | HCID 3072 | 47% |
Reaktionsschritte
A 500 mL three-neck flask was charged with the crude chloromethylether 1 (317 g, 2.00 mol). Triisopropylphosphite (494 mL) was added dropwise through an additional funnel while heating in a 125° C. oil bath and stirring vigorously. Collect 2-chloropropane distillate via short-path head in a dry ice cooled receiver, argon blanket, collected 140 g distillate (theoretical 157 g). Phosphite blanched reaction to yellow, continue heating another 2 h at 125° C. oil bath, then arrange for vacuum distillation using a vacuum pump. Distilled a yellow front cut (140 g, head to 135° C., bottom to 190° C.), then changed to clean receiver. Main fraction was collected at head temperature of 178-187° C. (mostly 185-187° C.) with vacuum unknown at bath temperature of 222-228° C. 258 g of the product 2 was given (47% yield from 1,3-dioxolane).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08088754B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-a26f559d1f7e48569a465696f70f09e1 |
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| Quellennotiz | uspto-grants-2012_01 |
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