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1-(2-Hydroxy-5-fluorophenyl)ethanol synthesis

2synthesis methods
-

Yield:850793-83-8 94%

Reaction Conditions:

in tetrahydrofuran;diethyl ether at -78 - 20; for 0.5 h;

Steps:

82.B

Step B MeMgBr (10 mL, 3 M solution in Et20) is added to a-78 °C cooled solution of aldehyde (2 g, 14.285 mmol) in THF (30 mL). The mixture is allowed to reach r. t. , stirred for 30 min. and poured into brine. It is acidified with diluted HCI and extracted with EtOAc. The organic layer is dried, filtered and concentrated, to give a crude residue that is purified by flash chromatography on Si02 (10-15% EtOAc/hexanes) to afford 2.1 g of the addition product (94%, colorless oil).

References:

WO2005/37763,2005,A1 Location in patent:Page/Page column 126

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