反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 100 °C
PROCEDURE
实验过程
Amine-containing enol ether copolymers (i.e. Poly(alkyl enolether-co-vinyloxy ethylamine) Polymers: 2-(vinyloxy)ethyl phthalimide (ImVE) was prepared by reacting 2-chloroethyl vinyl ether (25 g, 0.24 mol) with potassium phthalimide (25 g, 0.135 mol) in dimethyl foramide (75 mL) using tetra-n-butyl ammonium bromide as a phase transfer catalyst. This reaction mixture was stirred at 100° C. for 6 h then poured into 800 mL distilled water, and filtered and washed with a large amount of distilled water. The recovered yellowish crystals where then recrystallized twice from methanol to give white crystals, which were then dried for 48 h under reduced pressure. Polymerization was carried out in anhydrous methylene chloride at −78° C. under a blanket of dry nitrogen gas in oven-dried glassware. The reaction was initiated by adding borontrifluoride diethyl etherate to ImVE, and a mixture of enol ethers. The reaction was allowed to run for 3 h at −78° C., and then allowed to warm for ten minutes at RT, and then quenched with prechilled ammonia saturated methanol. The product was then evaporated to dryness under reduced pressure to give the product polymers. The polymer was then dissolved in a 1,4-dioxane(2)/methanol mixture and 10 equivalents (eq.) of hydrazine hydrate per mole of amine present. This solution was then refluxed for 2 h, cooled to RT, and the solvent was then removed under reduced pressure. This solution was then brought up in 0.5M HCl, and refluxed for 60-minutes. The cooled solution was then transferred to 3,000 MW dialysis tubing and dialyzed (4×5 L) for 48 h. This solution was then frozen and lyophilized. The following polymers were generated using this procedure:
WORKUP
后处理
- additionthen poured into 800 mL
- distillationdistilled water
- filtrationfiltered
- washwashed with a large amount of distilled water
- customThe recovered yellowish crystals where then recrystallized twice from methanol
- customto give white crystals, which
- customwere then dried for 48 h under reduced pressure
- customPolymerization
- waitto run for 3 h at −78° C.
- temperatureto warm for ten minutes at RT
- customquenched with prechilled ammonia saturated methanol
- customThe product was then evaporated to dryness under reduced pressure
- customto give the product polymers
- temperatureThis solution was then refluxed for 2 h
- temperaturecooled to RT
- customthe solvent was then removed under reduced pressure
- temperaturerefluxed for 60-minutes
- customThe cooled solution was then transferred to 3,000 MW dialysis tubing
- customdialyzed (4×5 L) for 48 h
- temperatureThis solution was then frozen