戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 640500作成日:2026年10月26日

Tetrahydrofuran → Tributyl(iodomethyl)stannane

https://huagongshe.com/reaction/640500

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物TriphenylphosphineHCID 11776—
反応物N-IodosuccinimideHCID 120273—
反応物1-(Tributylstannyl)methanolHCID 4193593—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物Tributyl(iodomethyl)stannaneHCID 1086292694.9%

反応条件

温度0 °C

反応手順

To a mixture of triphenylphosphine (70 g, 0.27 mol) and tetrahydrofuran (500 mL) was added dropwise a mixture of N-iodosuccinimide (60 g, 0.27 mol) and tetrahydrofuran (500 mL) at 0° C., and then the reaction mixture was stirred for 30 minutes at 0° C. To this mixture was added dropwise tributylstannyl-methanol (71 g, 0.22 mol) described in Manufacturing Example 197-2-1 at 0° C., and then the reaction mixture was stirred for 20 minutes at 0° C. The reaction mixture was stirred overnight at room temperature. Diethyl ether and water were added to the reaction mixture, and the organic layer was separated. The organic layer was washed first with a saturated sodium thiosulfate aqueous solution and then with saturated aqueous sodium chloride. The organic layer was separated, and was concentrated under a reduced pressure. Heptane (400 mL) was added to the residue and filtered. The solvent in the filtrate was evaporated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane) to obtain the title compound (90 g, 94%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691882B2
出典データセットuspto-grants-2010_04
ORD IDord-0c4f06f723274c7891d43ebb0187fc57
出典メモuspto-grants-2010_04