中因石油大学 CHINA UNIVERSITY OF PETROLEUM 1.醚的自氧化(-氢的氧化) R一 02(空气) R R- COR OOH 过氧化物 提示: 醚类试剂(乙醚、THF等)久置使用时要当心 ·先用淀粉一KI(2%的醋酸溶液)试验 蒸馏时勿蒸干 可用还原剂处理除去过氧化物(如FeSO4,NaHSO,等) 7143
7/43 1. 醚的自氧化(α-氢的氧化) 提示:醚类试剂(乙醚、THF等)久置使用时要当心 • 先用淀粉-KI(2%的醋酸溶液)试验 • 蒸馏时勿蒸干 • 可用还原剂处理除去过氧化物(如FeSO4,NaHSO3等) R' C O R H H O2(空气) R' C O R H OOH 过氧化物
中因石油大学 CHINA UNIVERSITY OF PETROLEUM 2.1 醚的碱性 样盐 R一OR'+HCI R—O—R' H ① R一0-R'+H2S04 R一OR' HSO4 H BH3 BH3 Et 酸碱络合物 Et 稳定RMgX和BH,等活泼的试剂 8/43
8/43 2. 醚的碱性 M g R X Et O Et Et O Et R O R' HCl R O R' H + Cl R O R' H2SO4 R O R' H + HSO4 O O BH3 + BH3 酸碱络合物 钅羊盐 稳定RMgX和BH3等活泼的试剂
中因石油大学 CHINA UNIVERSITY OF PETROLEUM 3. 醚键的开裂(醚在酸性体系中的亲核取代) 醚键在中性、碱性或弱酸性条件下不会断裂。 醚键可被HⅡ和HB在加热下断裂 HX ROR R一X+ HO-R" △ X=I,Br X过量时,生成 2分子卤代烷 9143
9/43 3. 醚键的开裂(醚在酸性体系中的亲核取代) 醚键在中性、碱性或弱酸性条件下不会断裂。 醚键可被 HI 和 HBr 在加热下断裂 R O R' HX R X + HO R' X = I, Br HX过量时,生成 2分子卤代烷
中因石油大学 CHINA UNIVERSITY OF PETROLEUM 例: H3C. H3C HCCH-OH 1(过量)之 H3C 48%HBr(过量) △ o- OH 1,4-二溴丁烷 10143
10/43 H3C CH H3C O CH CH3 CH3 H3C CH H3C I O 48% HBr(过量) Br OH Br Br + H3C CH H3C OH H3C CH H3C I H I H I(过量) 2 例: H3C CH H3C O CH CH3 CH3 H3C CH H3C I O 48% HBr(过量) Br OH Br Br + H3C CH H3C OH H3C CH H3C I H I H I(过量) 2 1,4-二溴丁烷 H3C CH H3C O CH CH3 CH3 H3C CH H3C I O 48% HBr(过量) Br OH Br Br + H3C CH H3C OH H3C CH H3C I H I H I(过量) 2 H3C CH H3C O CH CH3 CH3 H3C CH H3C I O 48% HBr(过量) Br OH Br Br + H3C CH H3C OH H3C CH H3C I H I H I(过量) 2
中因石油大学 CHINA UNIVERSITY OF PETROLEUM 不对称醚醚键的开裂取向 CH3CH2-OH I-CH2CH2CH3 HI CH3CH2>O-CH2CH2CHs CH3CH2-l HO-CH2CH2CH3 基团体积差别不大 混合物 HI H3 CH2CH2CH3 CH3-l HO-CH2CH2CH3 4 小 1o较大 烃基小的得到卤代烷 11/43
11/43 不对称醚醚键的开裂取向 基团体积差别不大 CH3CH2 O CH2CH2CH3 CH3CH2 OH + I CH2CH2CH3 CH3CH2 I + HO CH2CH2CH3 HI CH3 O CH2CH2CH3 HI CH3 I + HO CH2CH2CH3 CH3 O C CH3 CH3 HI CH3 OH + CH3 O CH3 CH3 H HI CH3 I + HO CH3 CH3 H CH3 I C CH3 CH3 CH3 CH3CH2 O CH2CH2CH3 CH3CH2 OH + I CH2CH2CH3 CH3CH2 I + HO CH2CH2CH3 HI CH3 O CH2CH2CH3 HI CH3 I + HO CH2CH2CH3 CH3 O C CH3 CH3 HI CH3 OH + CH3 O CH3 CH3 H HI CH3 I + HO CH3 CH3 H CH3 I C CH3 CH3 CH3 小 1 o 较大 混合物 烃基小的得到卤代烷 CH3CH2 O CH2CH2CH3 CH3CH2 OH + I CH2CH2CH3 CH3CH2 I + HO CH2CH2CH3 HI CH3 O CH2CH2CH3 HI CH3 I + HO CH2CH2CH3 CH3 O C CH3 CH3 HI CH3 OH + CH3 O CH3 CH3 H HI CH3 I + HO CH3 CH3 H CH3 I C CH3 CH3 CH3 CH3CH2 O CH2CH2CH3 CH3CH2 OH + I CH2CH2CH3 CH3CH2 I + HO CH2CH2CH3 HI CH3 O CH2CH2CH3 HI CH3 I + HO CH2CH2CH3 CH3 O C CH3 CH3 HI CH3 OH + CH3 O CH3 CH3 H HI CH3 I + HO CH3 CH3 H CH3 I C CH3 CH3 CH3