摘要
We reported a facile synthesis of (-)-isochrysanthenone(2) from (-)-α-pinene in a high yield. When (-)-α-pinene reacted with O 2 in the presence of Co[4-Me(C 5H 4N) 2]Br 2 used as a catalyst, the crude product of (-)-verbenone(1) was formed, and the crude product 1 was directly irradiated with ultraviolet light and converted into the (-)-isochrysanthenone(2). The structure of compound 2 was converted to a cyclic ester(4) by Baeyer-Villiger oxidation, the compound 4 was hydrolyzed to form a crystal 2,2,4-trimethyl-5-oxy-3-cyclohexenyl carboxylic acid 5. Compound 5 was confirmed by IR, 1H NMR and X-ray crystal analysis. In summary, we found that under the condition of photochemical rearrangement of (-)-verbenone and (+)-verbenone, different compounds were obtained, they are not enantiomers.
We reported a facile synthesis of (-)-isochrysanthenone(2) from (-)-α-pinene in a high yield. When (-)-α-pinene reacted with O 2 in the presence of Co[4-Me(C 5H 4N) 2]Br 2 used as a catalyst, the crude product of (-)-verbenone(1) was formed, and the crude product 1 was directly irradiated with ultraviolet light and converted into the (-)-isochrysanthenone(2). The structure of compound 2 was converted to a cyclic ester(4) by Baeyer-Villiger oxidation, the compound 4 was hydrolyzed to form a crystal 2,2,4-trimethyl-5-oxy-3-cyclohexenyl carboxylic acid 5. Compound 5 was confirmed by IR, 1H NMR and X-ray crystal analysis. In summary, we found that under the condition of photochemical rearrangement of (-)-verbenone and (+)-verbenone, different compounds were obtained, they are not enantiomers.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2004年第11期2119-2121,共3页
Chemical Journal of Chinese Universities
基金
国家自然科学基金 (批准号 :2 0 172 0 19)资助
