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note
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General procedure for the synthesis of 1-chloro-2-formyl indenes and tetralenes: Indanone Or tetralone (2 mmol) was taken in dry dimethylformamide (1 mL) and stirred at 0-10°C in an ice bath. To this phosphorus oxychloride (0.5 mL, 836 mg, 5.43 mmol) was added and further stirred for 1 h. On completion, the reaction mixture was poured in crushed ice, extracted with ethyl acetate, washed with water. The organic layer was dried over anhydrous sodium sulphate and evaporated in vacuo. The desired 1-chloro-2-formyl indenes/tetralenes were obtained either solid or oil. In some of the cases chromatographic purification was done through silica gel column and hexane-ethyl acetate as eluents.
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16
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79958736809
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note
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+. (Chemical Equation Presented)
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17
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Srivastava, V.; Darokar, M. P.; Fatima, A.; Kumar, J. K.; Chowdhury, C.; Dwivedi, G. R.; Shrivastava, K.; Gupta, V.; Chattopadhyay, S. K.; Luqman, S.; Saxena, H. O.; Gupta, M. M.; Negi, A. S.; Khanuja, S. P. S. Bioorg. Med. Chem. 2007, 15, 518.
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