Phenol → Phenol, 4-((2-chloro-5-iodophenyl)methyl)-

Temperature

22.5 °C

A 100 mL of 4-necked flask equipped with thermometer and mechanical stirrer was charged with (2-chloro-5-iodophenyl)methanol (268.5 mg, 1 mmol), anhydrous ZnCl2 (136.3 mg, 1 mmol), dichloromethane (5.0 mL) and n-hexane (29 mL) under argon. After stirring for 10 min at 20 to 25° C., HBr (gas) was bubbled into the mixture for 10 min and a solution of phenol (197.6 mg, 2.1 mmol) in dry dichloromethane (3.0 mL) was added dropwise over 30 min. After bubbling HBr for additional 2 h, the mixture was refluxed for 3 days. The conversion was about 65%. The mixture was quenched with ice water (50 mL), extracted with ethyl acetate (2×30 mL), washed with water (2×30 mL), brine (30 mL), concentrated and the residue was purified by flash chromatography (PE:EA=25:1 as eluant, 200 mL) to give an off-white solid. Yield: 180 mg (52%). 1H NMR (CDCl3, 400 MHz): δ 7.44 (d, J=8.4 Hz, 2H), 7.03˜7.09 (m, 3H), 6.77 (d, J=8.4 Hz, 2H), 4.76 (s, 1H), 3.95 (s, 2H), 3.82 (s, 2H). MS ESI (m/z): 345 [M+1]+. 13C NMR (CDCl3, 100 MHz): δ 154.1, 141.4, 139.5, 136.6, 134.2, 131.2, 130.9, 130.1, 115.5, 91.67, 38.07.

1. customA 100 mL of 4-necked flask equipped with thermometer and mechanical stirrer
2. customHBr (gas) was bubbled into the mixture for 10 min
3. customAfter bubbling HBr for additional 2 h
4. temperaturethe mixture was refluxed for 3 days
5. customThe mixture was quenched with ice water (50 mL)
6. extractionextracted with ethyl acetate (2×30 mL)
7. washwashed with water (2×30 mL), brine (30 mL)
8. concentrationconcentrated
9. customthe residue was purified by flash chromatography (PE:EA=25:1 as eluant, 200 mL)
10. customto give an off-white solid

ORD record

ord-4a95912dc1b74ba1931fbc8e8559fe56

Source dataset

uspto-grants-2015_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09193751B2