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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 640500생성일: 2026년 10월 24일

Tetrahydrofuran → Tributyl(iodomethyl)stannane

https://huagongshe.com/ko/reaction/640500

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물TriphenylphosphineHCID 11776—
반응물N-IodosuccinimideHCID 120273—
반응물1-(Tributylstannyl)methanolHCID 4193593—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물Tributyl(iodomethyl)stannaneHCID 1086292694.9%

반응 조건

온도0 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691882B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-0c4f06f723274c7891d43ebb0187fc57
출처 메모uspto-grants-2010_04