Iodine → (4-Methoxy-3-nitro-phenyl)-(3,4-dimethoxy-phenyl)-methanol

Grignard reagent was prepared in an oven-dried three necked flask outfitted with a reflux condenser, dropping funnel, and magnetic stirrer. Approximately 3 mL of a solution of 3,4-bromoveratrole (3.5 g, 15.9 mmol) in THF (10 mL) was added to a mixture of magnesium turnings (0.4 g, 15.9 mmol) in THF (5 mL) with a small piece of iodine. As soon as the solution became colorless (heating sometimes necessary), the remaining 3,4-bromoveratrole solution was added dropwise to the solution under mild reflux. The resulting mixture was refluxed for 3 h then cooled to room temperature for 30 min. The (3,4-dimethoxyphenyl)magnesium bromide was then added slowly to a stirred solution of 4-methoxy-3-nitro-benzaldehyde (2.4 g, 13.3 mmol) in THF (10 mL) at 0° C. After complete addition, the solution was allowed to stir at room temperature for 1 h. The mixture was cooled to 0° C. and quenched with saturated NH4Cl solution (40 mL). The aqueous layer was extracted with EtOAc (3×20 mL). The combined organic layers were washed with water (2×30 mL), brine (30 mL) and dried (MgSO4). Solvent was removed and residue was purified by flash chromatography (silica gel, CH2Cl2:EtOAc 9:1) to give (4-methoxy-3-nitro-phenyl)-(3,4-dimethoxy-phenyl)-methanol as an oil (2.6 g, 63%): 1H NMR (CDCl3) δ 7.89 (d, J=2 Hz, 1H), 7.54-7.49 (dd, J=2, 8 Hz, 1H), 7.05 (d, J=8 Hz, 1H), 6.88-6.81 (m, 3H), 5.78 (d, J=3 Hz, 1H), 3.94 (s, 3H), 3.87 (s, 3H), 3.85 (s, 3H), 2.38 (d, J=3 Hz, 1H).

1. customan oven-dried three necked flask
2. customoutfitted with a reflux condenser
3. additionwas added dropwise to the solution under mild reflux
4. temperatureThe resulting mixture was refluxed for 3 h
5. additionAfter complete addition
6. temperatureThe mixture was cooled to 0° C.
7. customquenched with saturated NH4Cl solution (40 mL)
8. extractionThe aqueous layer was extracted with EtOAc (3×20 mL)
9. washThe combined organic layers were washed with water (2×30 mL), brine (30 mL)
10. dry with materialdried (MgSO4)
11. customSolvent was removed
12. customresidue was purified by flash chromatography (silica gel, CH2Cl2:EtOAc 9:1)

ORD 기록

ord-7533e4afdfa6436f8c1a075702da48b3

출처 데이터셋

uspto-grants-2007_12

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07312241B2