1. lec91 Hetero cyclic Analogues of Naphthalene with one heteroatom The most investigated compound of this group contain a nitrogen atom, and theoretically can be drived from naphthalene by the substation of carbon or carbon and hydrogen atoms by a nitrogen atom.The same result can be obtained by fusing a benzene on to that of pyridine and three structure result.Derivative of all three ring system 1, 2, 3 occure naturally in the form of alkaloide

2. lec92 These three type of compound are essentially aromatic in character.The oxygen analogues of naphthalene which will be considered here are those derived from benzopyrylium cation (4) and benzopyranes (5) and (6) derivatives of these systems occure widely in plants and the anthocyanins. subistituted benzopyrylium salt are responsible for most red and blue flower coloure.very few sulphur analogues are known and at present they are not of general interest.

3. lec93 Physical properties and structure CHO NH 2 + | CHO CH 3 NaOH N H 2 O 2 N HOOC HOOC or KMnO 4 (1) (2) O 3 N 3 O 3 O | CHO CHO N OHC OHC + diozonide glyoxal pyridine 2,3 - dicarbaldehyde 2 - amino benzaldehyde Quinoline is a colourless liquid its b.p 237cº it's miscible with most organic solvent,its useful high – boiling solvent for many types of organic compound.The structure for quinoline was first proposed by korner,and was supported at an early stage by an oxidation to quinolinic acid (2) and by several syntheses of which Friedlander's is shown.

4. lec94 ozone attacke quinoline at the 5,6 and 7,8 position the initial product is a diozonide, decomposition of diozonide give pyridine 2,3 – dicarbaldehyde and glyoxal 2 The resonance energy of quinoline (47.3) kcal/ mol calculated from heat of combustion data the position of quinoline ring are usually numbered as structure.

5. lec95 Chemical reaction 1 – basicity Quinoline is a slightly weaker base than pyridine and form many salt which sparingly soluble in water.

6. lec96 Quinoline is a colourless liquid, it form 1 – oxide with hydrogen peroxide and acetic acid and quaternary salt with methyl iodide which with alkali give the hydroxide these are in equilibrium with the corresponding bases (3) which can be tautomerize to an open – chain (4) the oxidation of (3)give (5). Addition and ring – opening reactions :

7. lec97

8. 8 N Me 2 + OH - Na/Hg Emde's methods N Me 2 3 - phenyl - N - dimethyl- Propane amine N OH H H H Me 2 -H 2 O Me 2 N Me N + MeOH O - propene - N - dimethylaniline 160 15 mm ordinary pressure

9. lec99 Reduction : Quinoline is easily reduced to tetrahydroquinoline by tin and hydrochloric acid or by hydrogenation.

10. lec910 Oxidation : Oxidation of quinoline opens the ring giving quinolinic acid (1) the 2 – phenyl quinoline (2) and hydroxide (3) the nitrogen – containing ring can be split

11. lec911 Mechanism

12. lec912 Substitution reaction The nitrogen atom deactivates the pyridine ring and so the subistituent enter the benzene ring.calculation of charge densities show that position 8 will be attack by electrophilic reagent and position -2- by nucleophilic reagents.In practice nitration and sulphonation give a mixture of – 5 and 8 – substituted product. In bromination the heterocyclic rings is subistituted in the 3 – position.

13. lec913 + Quinoline resonance hybrid indicate the same result for electrophilic and nucleophilic substituent.

14. lec914 Electrophilic subistitution

15. lec915 Nucleophilic subistitution

16. lec916 Synthesis of quinoline 1 – Skraup's synthesis It is the most useful method for preparing quinoline from aniline and glycerol in presence of concentrated sulphuric and nitrobenzene.

17. lec917 The following steps seem to be involved + 1 – Dehydration of glycerol by hot sulphuric yield the unsaturated aldehyde acroline.

18. lec918 β­ ( phenylamino) propionaldehyde 2 – Nucleophilic addition of aniline to acrolein to yield β – (phenylamino) – propionaldehyde.

19. lec919 3 – Electrophilic attacke on the aromatic ring by the electron deficient carbonyl carbon of the protonated aldehyde.

20. lec920 4 – Oxidation by nitrobenzene resulting in the aromatization of the new formed ring