Triphenylphosphine → 4-(5-bromo-2-fluorophenoxymethyl)-1-methyl-1H-[1,2,3]triazole

An ice-cooled solution of 5-bromo-2-fluorophenol (1.91 g, 10 mmol), (1-methyl-1H-[1,2,3]triazol-4-yl)methanol (1.24 g, 11 mmol) and triphenylphosphine (3.93 g, 15 mmol) in tetrahydrofuran (50 ml) was treated dropwise with diisopropyl azodicarboxylate (3.03 g, 15 mmol) over 10 min. The resulting mixture was stirred to ambient temperature over 12 h and then glacial acetic acid (1 ml) was added. The reaction mixture was concentrated in vacuo then partitioned between ethyl acetate and 0.01N sodium hydroxide solution. The organics were washed with water, brine, dried over anhydrous magnesium sulphate and concentrated to give an oil. This oil was purified by chromatography on silica gel, eluting with isohexane on a gradient of ethyl acetate (20-50%). Product-containing fractions were concentrated and the resulting residue triturated with 10% ether in isohexane to furnish 4-(5-bromo-2-fluorophenoxymethyl)-1-methyl-1H-[1,2,3]triazole as a white solid (1.9 g, 66%): δH (360 MHz, d6-DMSO) 4.06 (3H, s), 5.25 (2H, s), 7.10-7.20 (2H, m), 7.55-7.70 (1H, m), 8.19 (1H, s).

1. concentrationThe reaction mixture was concentrated in vacuo
2. customthen partitioned between ethyl acetate and 0.01N sodium hydroxide solution
3. washThe organics were washed with water, brine
4. dry with materialdried over anhydrous magnesium sulphate
5. concentrationconcentrated
6. customto give an oil
7. customThis oil was purified by chromatography on silica gel
8. washeluting with isohexane on a gradient of ethyl acetate (20-50%)
9. concentrationProduct-containing fractions were concentrated
10. customthe resulting residue triturated with 10% ether in isohexane

ORD record

ord-69547399c72c4e81b85d8b7ec48a281b

Source dataset

uspto-grants-2007_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07279580B2