Tributylstannane → Stannane, tributyl(methoxymethyl)-

To a mixture of diisopropylamine (9.4 ml, 67 mmol) and tetrahydrofuran (150 ml) was added dropwise n-butyllithium (2.4M n-hexane solution, 25 ml, 61 mmol) at −78° C. (external temperature) Then, the reaction mixture was stirred for 30 minutes. To the mixture was added dropwise tributyltin hydride (16 ml, 61 mmol) at −78° C. (external temperature). Then, the reaction mixture was stirred at 0° C. (external temperature) for 30 minutes. After the reaction mixture was cooled at −78° C. (external temperature), chloromethyl methyl ether (4.6 ml, 61 mmol) was added dropwise to the reaction mixture. After the mixture was stirred at room temperature (external temperature) for 1 hour, water and diethyl ether were added to the reaction mixture, and the organic layer was separated. The organic layer was washed with an aqueous saturated sodium chloride solution, and the solvent was distilled off under reduced pressure. The residue was purified by neutral silica gel column chromatography (heptane:ethyl acetate=30:1) to obtain the title compound (18 g, 0.52 mmol, 86%).

1. stirringThen, the reaction mixture was stirred at 0° C. (external temperature) for 30 minutes
2. additionwas added dropwise to the reaction mixture
3. stirringAfter the mixture was stirred at room temperature (external temperature) for 1 hour
4. customthe organic layer was separated
5. washThe organic layer was washed with an aqueous saturated sodium chloride solution
6. distillationthe solvent was distilled off under reduced pressure
7. customThe residue was purified by neutral silica gel column chromatography (heptane:ethyl acetate=30:1)

ORD record

ord-4372bfaf515843e48714f5992dbb067c

Source dataset

uspto-grants-2010_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07696347B2