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HRID 715975作成日:2026年10月26日

Tributyltin Chloride → Tert-butyl 2-tributylstannanylethynylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/715975

反応式

関与物質

役割名称HCID仕込み量
反応物Tributyltin ChlorideHCID 15096—
反応物tert-Butyl 2-ethynylpyrrolidine-1-carboxylateHCID 14730283—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 2-tributylstannanylethynylpyrrolidine-1-carboxylateHCID 7098458461.2%

反応条件

温度-30 °C

反応手順

n-Butyllithium (1.6M in hexanes, 12.3 mL) was added over 2 minutes to a stirred solution of tert-butyl 2-ethynylpyrrolidine-1-carboxylate (3.65 g) in anhydrous THF (80 mL) at −78° C. under nitrogen and then the mixture was allowed to warm to −30° C. over one hour. Tributyltin chloride (6.41 g) was then added dropwise at −30° C. and the mixture was allowed to warm to −10° C. and quenched by addition of saturated sodium bicarbonate solution. The layers were separated and the organic layer was dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-5% to give tert-butyl 2-tributylstannanylethynylpyrrolidine-1-carboxylate (5.54 g) as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187494B2
出典データセットuspto-grants-2015_11
ORD IDord-776f43b0be0942e2b951c2f0e804c936
出典メモuspto-grants-2015_11