Terpenoids -module6
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Camphor is a bicyclic compound primarily derived from the camphor tree, with a molecular formula of C10H16O and characteristics indicating its saturated nature. Its structure includes a cyclic ketone functional group, which enables the formation of various derivatives such as camphoric acid and camphoronic acid upon oxidation and other chemical reactions. Camphor has two chiral centers resulting in a single pair of enantiomers, with its derivatives exhibiting specific conformational arrangements.
Terpenoids -module6
- 1. Camphor a) Source: It is a main constituent of camphor oil obtained from the wood and leaves of the camphor tree (Cinnamomum camphora) b) Structure of camphor: 1) Molecular formula: From analytical data and molecular weight determination, it follows that the molecular formula of camphor is C10 H16 O. 2) Saturated characteristics: Camphor does not add with bromine. However, it forms monosubstitution products like mono-bromocamphor etc. The formation of these products reveals that camphor is a saturated compound and does not contain any double bond. This is further supported by the facts that (i) it does not react with 1% alk. KMnO4 and (ii) molecular refraction also favours this. 3) Presence of a keto group: The nature of oxygen atom is found to be cyclic ketonic on the basis of following facts. i) It forms an oxime with hydroxylamine C10 H16 O + H2 NOH C10 H16 = N - OH Camphor Camphor oxime ii) It forms semicarbazone with semicarbazide. iii) It forms phenylhydrazone with phenylhydrazine. iv) Camphor when oxidised with nitric acid, yields a dicarboxylic acid called camphoric acid without loss of carbon atoms. Further, camphor when reduced with sodium amalgam, yields a secondary alcohol called borneol. Hence, camphor must be a cyclic ketone. v) When camphor is distilled with iodine, it yields carvacrol. The presence of phenolic group in carvacrol reveals the presence of ketonic group in camphor.
- 2. 4) Bicyclic system: The molecular formula of saturated parent hydrocarbon of camphor is C10 H18 which corresponds to the general formula Cn H2n-2 of bicyclic compounds and, therefore, camphor is a bicyclic compound. 5) Presence of -CH2 CO group: When camphor is treated with amyl nitrite and hydrochloric acid, it yields an iso-nitroso (oximino) camphor in which two hydrogen atoms have been replaced by = NOH group. This reaction reveals that the >C=O group is directly attached to a -CH2 group. 6) Presence of a six-membered ring: When camphor is distilled with zinc chloride or phosphorus pentoxide, it yields p-cymene. The formation of the latter product reveals the presence of six-membered ring, methyl and gem-dimethyl groups in camphor. 7) Nature of the carbon-frame in camphor: When camphor is oxidised with nitric acid, it yields a crystalline dibasic acid, camphoric acid, C10 H16 O4 . As camphoric acid possesses the same number of carbon atoms as camphor, it means that the keto group must be present in one of the rings in camphor. Thus, during the conversion of camphor into camphoric acid, the opening of ring containing the keto group occurs and therefore, camphoric acid must be a monocyclic compound. When camphoric acid is further oxidised with nitric acid, camphoronic acid is obtained. Camphor 3HNO Camphoric acid 3HNO Camphoronic acid C10 H16 O C10 H16 O4 C9 H14 O6 In order to elucidate the structure of camphor, the structure of camphoric acid and camphoronic acid should be known.
- 3. 8) Structure of camphoronic acid: This can be elucidated as follows: a) The molecular formula of camphoronic acid is C9 H14 O6 b) As camphoronic acid has been shown to be a saturated tricarboxylic acid, its molecular formula may be written as C6 H11 (COOH)3 and its parent hydrocarbon will, therefore, be C6 H14 which corresponds to the general formula (Cn H2n+2 ) for acyclic compound, indicating that camphoronic acid is an acyclic compound. c) As camphoronic acid does not undergo decarboxylation under ordinary conditions, it means that its three carboxyl groups should be attached to three different carbon atoms. d) When camphoronic acid is distilled at atmospheric pressure, it yields isobutyric acid (II), trimethylsuccinic acid (III) and carbon dioxide as the major products. In order to explain the formation of these products, Bredt suggested that camphoronic acid is - tricarballylic acid (I). 9) Synthesis of camphoronic acid: The structure (I) for camphoronic acid has been confirmed by its following synthesis.
- 4. 10) Structure of camphoric acid: It is elucidated as follows: a) The molecular formula of camphoric acid is C10 H16 O4 . b) By usual tests, camphoric acid has been shown to be a saturated dicarboxylic acid. c) Camphor is bicyclic . During the oxidation of camphor into camphoric acid, the ring containing the keto group gets opened and hence camphoric acid should be monocyclic. d) As camphoric acid is able to form a monoester readily but it forms diester with difficulty, this shows that the two carboxyl groups are not similar, i.e., one is primary or secondary and the other it tertiary. This is confirmed by the fact that camphoric anhydride forms only one monobromo derivative with phosphorus / bromine. The formation of this monobromo derivative is only possible if one of the carboxyl groups is secondary, ie. the carbon atom of one carboxyl groups must be 1 C. e) On the basis of the above facts the structure of camphoric acid may be given as follows.
- 5. 10) Synthesis of ( ) - camphoric acid: This involves the conversion of 3, 3-dimethyl- glutaric ester into camphoric acid as follows: 11) Structure of camphor: On the basis of the foregoing discussion the structure of camphor may be given as either III or IV. 12) Camphor gives carvacrol on distillation with iodine. This is possible only from structure III and not form structure IV.
- 6. 13) Synthesis of camphor: The above structure (III) of camphor is proved by the following synthesis. Stereochemistry of camphor Camphor has two dissimilar chiral centres but only one pair of enantiomers is known. This is due to the fact that only the cis-form is possible; trans fusion of the gem- dimethylmethylene bridge to the cyclohexane ring is impossible. Thus only the enantiomers of the cis-isomer are known. Camphor and its derivatives exist in the boat conformation. Since the gem-dimethyl bridge must be cis, the cyclohexane ring must have the boat form.