Tributylstannane → Tributyl(ethoxymethyl)stannane

To a mixture of diisopropylamine (2.1 ml, 15 mmol) and tetrahydrofuran (30 ml) was added dropwise n-butyllithium (2.4M n-hexane solution, 5.0 ml, 12 mmol) at −78° C. (external temperature). Then, the reaction mixture was stirred for 30 minutes. To the mixture was added dropwise tributyltin hydride (3.3 ml, 12 mmol) at −78° C. (external temperature). Then, the reaction mixture was stirred at 0° C. (external temperature) for 40 minutes. The reaction mixture was cooled to −78° C. (external temperature), and ethoxymethyl chloride (1.1 ml, 12 mmol) was added dropwise to the reaction mixture. After the reaction mixture was raised to room temperature, to the reaction mixture were added diethyl ether and an aqueous ammonium chloride solution, 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:diethyl ether=30:1) to obtain the title compound (2.8 g, 7.9 mmol, 66%).

1. stirringThen, the reaction mixture was stirred at 0° C. (external temperature) for 40 minutes
2. additionwas added dropwise to the reaction mixture
3. customan aqueous ammonium chloride solution, and the organic layer was separated
4. washThe organic layer was washed with an aqueous saturated sodium chloride solution
5. distillationthe solvent was distilled off under reduced pressure
6. customThe residue was purified by neutral silica gel column chromatography (heptane:diethyl ether=30:1)

ORD record

ord-c2fcf8a571ed4736b4c20c9e826e6a74

Source dataset

uspto-grants-2010_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07696347B2