1. AZIRINE
One of the simplest heterocyclic compound or azacyclo propene. It could have structure 1 or II
Azirine found natmaly as a part of some compound such as III and IV
Which are used as an antibiotic and could be synthesis.
Which are used as an antibiotic and could be synthesis.
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2. Reactions:-
Methanol reacted by addition with 1- azririne to give 2- Methoxy azirine in presence of sodmethoxide as a catalyst.
3,3 – dimethyl -2- phynyl -1- azirine react with sulphonic acid.
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3. Reaction with acetic acid and acetic anhydride.
Reaction with Grignard reagent.
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4. Synthesis:-
From thermal analysis of Ethanyl azide which can be prepared from alkenes.
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5. Oxirane
Oxirane or ethylene oxide (1) it was first obtain by wartz in in 1931 P taent was taken out on direct oxidation of ethylene to okirane by oxygen. Oxiranes found naturally in a plant, animal and insect. Orapetene (2) was oxirane separated from natural source. In general orxirane ring found as a part of structure of many compound specially prostalandine.
Some oxirane drevative use as an antibiotic and its effective in treatment of malignant toummer.
- It is colourless liquide misible with water
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6. Chemical properties:-
1. When oxirane heated its rearranged to aldehyde.
2. Ring opening:-
The most important reaction of oxirane is the ring opening became its very important in organic synthesis.
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7. 3. Nucleophillic reagent:-
It react with oxirane such as ammonia to give mono ethanolamine in excess of oxirane it give diethanol amine and triethanol amine.
b - With Grignard reagent it give alcohol
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8. c – with halogen in presence of ph3p or lix give B- halo alcohol
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9. Reduction
Oxirane reduce to alcohol
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10. Electrophillic reactions:-
Polymarisation:-
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11. Synthesis:-
1. From B- Halo alcohol by elimination of hydrogen halide by base
2. Darzen reaction:-
halo ester with carbonyl compound in presence of sod. Ethoxide.
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12. Thirane Chemical reactions:-
It is known also as ethylene sulphide its highly strain ring less stable than oxirane. Substituted thirane more stable than un-substituted one.
It is colourless liquid in sulible in water but dissolve in organic solvent, boil at 55Co
Chemical reactions:-
1. it react with ammonia to give drevative of B- aminothiol
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13. 3. It react with sodium periodate to give thirane okide.
2. Nucleophilic reagent always attack carbon atom but in thirane it attack carbon atom but in thirane it attack the sulphur atom leading to alkene formation.
3. It react with sodium periodate to give thirane okide.
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14. This became the proton added to sulphur and carbonium ion formed.
4. Reduction
This became the proton added to sulphur and carbonium ion formed.
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15. Synthesis: -1- 1. From chlorothiol cyclised by sod. Bicarbonate
2. From okirane when treated with pot. Thiocyanate.
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16. Heterocyclic analogues of cyclobutane
Four membered ring are not highly strained as the corresponding three-membered rings. But are more difficult to prepare by the direct cyclisation of straight chain intermediate. The most important of four membered ring are Azetidine, oxetane and thietane.
Oxetanes:-
Synthesis
By cyclo addition of two double bond.
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17. Reaction
They are susceptible to acid catalyzed ring-opening reaction (like three membered ring analogues.
It react with nucleophilic reagent but are less reactive than the analogues three membered ring compounds.
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18. Azetidine
Synthesis:-
Similar to oxetanes preparation
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19. Thietanes
Syntesis:-
By ring closure similar to azetidine
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