(2S)-6-methyl-2-[(1S)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol

反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

実験手順: To the solution containing 1.25 g. of farnesyl carboxylic acid dissolved in 0.5 N ammonia water, 0.845 g. of silver nitrate in 3 ml. water was added. The resulting precipitate was collected by filtration and dried. The silver salt was powdered and suspended in 120 ml. of benzene, and distilled to about 60 ml. of benzene solution to remove the remaining water azeotropically. Separately, α-bisabolol chloride was prepared by adding triphenyl phosphine in an amount of 1.3 times the stoichiometric quantity, to α-bisabolol in a solution of carbon tetrachloride (1:8) and following 1 hour of reflux in water bath, the product was purified by vacuum distillation. The purified α-bisabolol chloride in an amount of 1.39 g. was dissolved in 3 ml. of benzene and added to the above solution of silver salt suspension which had been prepared previously. After 9 hours of reflux, the reaction mixture was washed with water and dried (sodium sulfate). The desired fraction was obtained by vacuum distillation (155°-156° C./0.1 mmHg) under N2 gas stream. To the solution containing 1.25 g The resulting precipitate was collected by filtration dried of benzene, and distilled to about 60 ml of benzene solution to remove the remaining water azeotropically the product was purified by vacuum distillation was dissolved in 3 ml of benzene and added to the above solution of silver salt suspension which had been prepared previously After 9 hours of reflux the reaction mixture was washed with water dried (sodium sulfate) The desired fraction was obtained by vacuum distillation (155°-156° C./0.1 mmHg) under N2 gas stream