Trimethyl borate → 2-Fluoro-3-iodobenzyl alcohol

Trimethyl borate (1.92 mL, 17.2 mmol) was added dropwise to a stirred solution of 2-fluoro-3-iodobenzoic acid (preparation 22b, 4.39 g, 16.5 mmol) in tetrahydrofuran (25 mL) at 0° C. and the mixture was stirred for a further 15 minutes at this temperature. Then borane-methyl sulfide complex (10 M, 4.4 mL, 44 mmol) in tetrahydrofuran (3 mL) was added dropwise to the mixture at 0° C. and the mixture was then allowed to warm to room temperature. After 1 hour, the mixture was carefully quenched by dropwise addition of methanol (10 mL). After stirring overnight, the mixture was concentrated in vacuo and ethyl acetate was added to the residue. The organic layer was washed with saturated aqueous potassium carbonate solution, brine, dried (MgSO4) and evaporated to give the title compound (4.03 g, 97%) as an oil.

1. waitAfter 1 hour
2. customthe mixture was carefully quenched by dropwise addition of methanol (10 mL)
3. stirringAfter stirring overnight
4. concentrationthe mixture was concentrated in vacuo and ethyl acetate
5. additionwas added to the residue
6. washThe organic layer was washed with saturated aqueous potassium carbonate solution, brine
7. dry with materialdried (MgSO4)
8. customevaporated

ORD record

ord-a3299156cbdd4da2b0436335fbd7808c

Source dataset

uspto-grants-2013_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08450341B2