Lithium Hexamethyldisilazide → 1-(3-Ethoxy-4-methoxy-phenyl)-1-(3-nitro-4-methoxy-phenyl)-ethene

To a stirred suspension of triphenylmethylphosphonium bromide (1.8 g, 5.1 mmol) in THF (30 mL) in an ice bath was added lithium bis(trimethylsilyl)amide (1.0M solution in THF, 5.1 mL, 5.1 mmol) dropwise. The mixture was stirred at room temperature for 40 min. The Wittig reagent was then added slowly to a stirred suspension of (4-methoxy-3-nitro-phenyl)-(3-ethoxy-4-methoxy-phenyl)-methanone (1.4 g, 4.2 mmol) in THF (30 mL) in an ice bath. The mixture was stirred at room temperature for 5 hr. The mixture was poured into ice water (100 mL). The aqueous layer was extracted with methyl chloride (4×30 mL). The combined organic layers were washed with water (2×50 mL), brine (50 mL) and dried (MgSO4). Removal of solvent and chromatography (silica gel) gave 1-(3-ethoxy-4-methoxy-phenyl)-1-(3-nitro-4-methoxy-phenyl)-ethene as a solid (0.9 g, 67% yield): 1H NMR (CDCl3) δ 1.44 (t, J=7.2 Hz, 3H, CH3), 3.89 (s, 3H, OCH3), 3.98 (s, 3H, OCH3), 4.10 (q, J=7.0 Hz, 2H, OCH2), 5.37 (d, J=9.7 Hz, 2H, CH2), 6.83-6.84 (m, 3H, CH), 7.06(d, J=8.9 Hz, 1H, CH), 7.49-7.54 (dd, J=2.3, 8.9 Hz, 1H, CH), 7.84 (d, J=2.1 Hz, 1H, CH); 13C NMR (CDCl3) δ 14.70, 55.94, 56.56, 64.35, 111.19, 112.74, 113.10, 113.68, 120.80, 125.11, 133.08, 133.66, 134.27, 139.42, 147.24, 148.03, 149.49, 152.30.

1. stirringThe mixture was stirred at room temperature for 5 hr
2. extractionThe aqueous layer was extracted with methyl chloride (4×30 mL)
3. washThe combined organic layers were washed with water (2×50 mL), brine (50 mL)
4. dry with materialdried (MgSO4)
5. customRemoval of solvent and chromatography (silica gel)

ORDレコード

ord-29d528e08e874bb8a6d8cd8134eff999

出典データセット

uspto-grants-2008_12

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07470723B2