乙基 (E)-4-苯基丁-2-烯酸乙酯

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: To a stirred suspension of LiAlH4 (2.4 g, 63.1 mmol) in dry Et2O (60 mL) at 0° C. under nitrogen atmosphere was added dropwise a solution of anhydrous AlCl3 (1.7 g, 12.6 mmol) in dry Et2O (30 mL). The reaction mixture was stirred at the same temperature for 30 min. To this stirred suspension, ester obtained in example 1 (8.0 g, 42.1 mmol) in dry Et2O (30 mL) was added dropwise over a period of 15 min and the resulting mixture stirred at 0° C. for 1 h. Then it was quenched with ice-water and filtered through celite and the residue was washed with ethyl acetate (3×30 mL). The combined organic layer was dried over anhydrous Na2SO4, concentrated, and the crude product was purified by column chromatography using petroleum ether/EtOAc (4:1) to afford the pure allylic alcohol 7 (5.4 g, 87%) as a colorless oil. IR: (CHCl3, cm−1): νmax 694, 744, 966, 1049, 1107, 1364, 1454, 2857, 2932, 3385; 1H NMR (200 MHz, CDCl3): δ 1.22 (br s, 1H), 3.38 (d, J=6.4 Hz, 2H), 4.12 (t, J=4.8 Hz, 2H), 5.62-5.93 (m, 2H), 7.15-7.32 (m, 5H); 13C NMR (50 MHz, CDCl3): δ 36.4, 61.9, 126.0, 126.3, 127.2, 128.5, 132.7, 137.2; Anal. Calcd for C10H12O: C, 81.04; H, 8.16. Found: C, 81.02; H, 8.15%. the resulting mixture stirred at 0° C. for 1 h Then it was quenched with ice-water filtered through celite the residue was washed with ethyl acetate (3×30 mL) The combined organic layer was dried over anhydrous Na2SO4 concentrated the crude product was purified by column chromatography

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: To a stirred suspension of LiAlH4 (2.4 g, 63.1 mmol) in dry Et2O (60 mL) at 0° C. under nitrogen atmosphere was added dropwise a solution of anhydrous AlCl3 (1.7 g, 12.6 mmol) in dry Et2O (30 mL). The reaction mixture was stirred at the same temperature for 30 min. To this stirred suspension, ester obtained in example 1 (8.0 g, 42.1 mmol) in dry Et2O (30 mL) was added dropwise over a period of 15 min and the resulting mixture stirred at 0° C. for 1 h. Then it was quenched with ice-water and filtered through celite and the residue was washed with ethyl acetate (3×30 mL). The combined organic layer was dried over anhydrous Na2SO4, concentrated, and the crude product was purified by column chromatography using petroleum ether/EtOAc (4:1) to afford the pure allylic alcohol 7 (5.4 g, 87%) as a colorless oil. IR: (CHCl3, cm−1): νmax 694, 744, 966, 1049, 1107, 1364, 1454, 2857, 2932, 3385; 1H NMR (200 MHz, CDCl3): δ 1.22 (br s, 1H), 3.38 (d, J=6.4 Hz, 2H), 4.12 (t, J=4.8 Hz, 2H), 5.62-5.93 (m, 2H), 7.15-7.32 (m, 5H); 13C NMR (50 MHz, CDCl3): δ 36.4, 61.9, 126.0, 126.3, 127.2, 128.5, 132.7, 137.2; Anal. Calcd for C10H12O: C, 81.04; H, 8.16. Found: C, 81.02; H, 8.15%. the resulting mixture stirred at 0° C. for 1 h Then it was quenched with ice-water filtered through celite the residue was washed with ethyl acetate (3×30 mL) The combined organic layer was dried over anhydrous Na2SO4 concentrated the crude product was purified by column chromatography

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: To a stirred suspension of LiAlH4 (2.4 g, 63.1 mmol) in dry Et2O (60 mL) at 0° C. under nitrogen atmosphere was added dropwise a solution of anhydrous AlCl3 (1.7 g, 12.6 mmol) in dry Et2O (30 mL). The reaction mixture was stirred at the same temperature for 30 min. To this stirred suspension, ester obtained in example 1 (8.0 g, 42.1 mmol) in dry Et2O (30 mL) was added dropwise over a period of 15 min and the resulting mixture stirred at 0° C. for 1 h. Then it was quenched with ice-water and filtered through celite and the residue was washed with ethyl acetate (3×30 mL). The combined organic layer was dried over anhydrous Na2SO4, concentrated, and the crude product was purified by column chromatography using petroleum ether/EtOAc (4:1) to afford the pure allylic alcohol 7 (5.4 g, 87%) as a colorless oil. IR: (CHCl3, cm−1): νmax 694, 744, 966, 1049, 1107, 1364, 1454, 2857, 2932, 3385; 1H NMR (200 MHz, CDCl3): δ 1.22 (br s, 1H), 3.38 (d, J=6.4 Hz, 2H), 4.12 (t, J=4.8 Hz, 2H), 5.62-5.93 (m, 2H), 7.15-7.32 (m, 5H); 13C NMR (50 MHz, CDCl3): δ 36.4, 61.9, 126.0, 126.3, 127.2, 128.5, 132.7, 137.2; Anal. Calcd for C10H12O: C, 81.04; H, 8.16. Found: C, 81.02; H, 8.15%. the resulting mixture stirred at 0° C. for 1 h Then it was quenched with ice-water filtered through celite the residue was washed with ethyl acetate (3×30 mL) The combined organic layer was dried over anhydrous Na2SO4 concentrated the crude product was purified by column chromatography