Presentation is loading. Please wait.

Presentation is loading. Please wait.

24.11 Preparation of Aryl Ethers. Typical Preparation is by Williamson Synthesis ONa + RXRXRXRX OROROROR NaX + SN2SN2SN2SN2.

Similar presentations


Presentation on theme: "24.11 Preparation of Aryl Ethers. Typical Preparation is by Williamson Synthesis ONa + RXRXRXRX OROROROR NaX + SN2SN2SN2SN2."— Presentation transcript:

1 24.11 Preparation of Aryl Ethers

2 Typical Preparation is by Williamson Synthesis ONa + RXRXRXRX OROROROR NaX + SN2SN2SN2SN2

3 Typical Preparation is by Williamson Synthesis ONa + RXRXRXRX OROROROR NaX + SN2SN2SN2SN2 but the other combination X + RONa fails because aryl halides are normally unreactive toward nucleophilic substitution

4 acetone heat Example ONa + CH 3 I OCH 3 (95%)

5 acetone, heat Example OHOHOHOH + (86%) H2CH2CH2CH2C CHCH 2 Br K 2 CO 3 OCH 2 CH CH 2

6 Aryl Ethers from Aryl Halides F NO 2 + KOCH 3 CH 3 OH 25°C OCH 3 NO 2 + KFKFKFKF (93%) nucleophilic aromatic substitution is effective with nitro-substituted (ortho and/or para) aryl halides

7 24.12 Cleavage of Aryl Ethers by Hydrogen Halides

8 Cleavage of Alkyl Aryl Ethers OArR H + O Ar R H Br Br –+ +

9 Cleavage of Alkyl Aryl Ethers OArR H + O Ar R H Br Br –+ + R Br + OAr H An alkyl halide is formed; never an aryl halide!

10 + Example OCH 3 OH OHOH (85-87%) CH 3 Br (57-72%) HBr heat

11 24.13 Claisen Rearrangement of Allyl Aryl Ethers

12 Allyl Aryl Ethers Rearrange on Heating OH CH 2 CH CH 2 OCH 2 CH CH 2 200°C (73%) allyl group migrates to ortho position

13 rewrite as Mechanism OCH 2 CH CH 2 O O H keto-to-enol isomerization OH

14 Claisen rearrangement is an example of a sigmatropic rearrangement. A  bond migrates from one end of a conjugated  electron system to the other. this  bond breaks this  bond forms “conjugated  electron system” is the allyl group Sigmatropic Rearrangement O O H

15 24.14 Oxidation of Phenols: Quinones

16 The most common examples of phenol oxidations are the oxidations of 1,2- and 1,4-benzenediols to give quinones. (76-81%) QuinonesOHOHOO Na 2 Cr 2 O 7, H 2 SO 4 H2OH2OH2OH2O

17 The most common examples of phenol oxidations are the oxidations of 1,2- and 1,4-benzenediols to give quinones. (68%) Quinones O O Ag 2 O diethyl ether OHOH CH 3

18 Alizarin (red pigment) Some quinones are dyes OO OH OH

19 Ubiquinone (Coenzyme Q) n = 6-10 involved in biological electron transport Some quinones are important biomolecules CH 3 O OO CH 3 n

20 Vitamin K (blood-clotting factor) Some quinones are important biomolecules O CH 3 O


Download ppt "24.11 Preparation of Aryl Ethers. Typical Preparation is by Williamson Synthesis ONa + RXRXRXRX OROROROR NaX + SN2SN2SN2SN2."

Similar presentations


Ads by Google