RARECHEM AL BD 1307 synthesis

Yield:252004-50-5 4.8 g (83%)

Reaction Conditions:

with hydrogenchloride;sodium borohydrid in tetrahydrofuran;ethanol;

Steps:

5 (4-Chloro-2,6-difluoro-phenyl)-methanol

(4-Chloro-2,6-difluoro-phenyl)-methanol To a mixture of 4-chloro-2,6-difluoro-benzaldehyde (5.7 g, 32 mmol), tetrahydrofuran (150 mL) and ethanol (20 mL) was added sodium borohydride (1.2 g, 32 mmol) at 0° C. The mixture was stirred for 30 minutes, warmed to ambient temperature, and additional sodium borohydride (0.40 g, 11 mmol) was added to drive the reaction to completion (TLC). The mixture was concentrated in vacuo, diluted with ether and treated cautiously with 1M aqueous HCl. The aqueous phase was extracted 3* with ether, and the combined organic layers were dried over MgSO₄, filtered and concentrated. Trituration of the residue with pentane afforded 4.8 g (83%) of (4-chloro-2,6-difluoro-phenyl)-methanol as a colorless solid. ¹H NMR (300 MHz, CDCl₃) δ7.04 (d, 2H, J=7.1 Hz), 4.73 (s, 2H) ppm.

References:

US6235764,2001,B1