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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7891생성일: 2026년 10월 24일

Tetramethyltin → HCID 21990863, 화합물

https://huagongshe.com/ko/reaction/7891

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참여 물질

역할이름HCID투입량
반응물TetramethyltinHCID 11661—
반응물TriphenylphosphineHCID 11776—
반응물Lithium ChlorideHCID 433294—
반응물4-Bromo-2-butyl-6-fluoro-5-methoxy-1-indanoneHCID 21990906—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
생성물HCID 21990863HCID 2199086324.5%

반응 조건

온도100 °C

반응 단계

A mixture of 4-bromo-2-butyl-6-fluoro-5-methoxy-1-indanone (1.86 g, 5.94 mmol), bis(triphenylphosphine)palladium(II) chloride (208 mg, 0.297 mmol), tetramethyltin (0.989 mL, 7.128 mmol), triphenylphosphine (156 mg, 0.594 mmol), lithium chloride (504 mg, 11.88 mmol), and anhydrous N,N-dimethyl-formamide (11.9 mL) was placed under a nitrogen atmosphere, stirred, and heated in an oil bath at 100° C. for 22 hours. After cooling to room temperature, the mixture was evaporated under vacuum. The residue in EtOAc (150 mL) was washed with water (4×100 mL) and brine (50 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (2.15 g). The crude product was purified by chromatography on EM silica gel 60 (2.5×29 cm column), eluting with CH2Cl2 (50 mL fore-run followed by 8 mL fractions). Fractions 20-28 were combined and evaporated under vacuum to provide 2-butyl-6-fluoro-5-methoxy-4-methyl-1-indanone (365 mg) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-270913168eb241f99a23be25455ccdcc
출처 메모uspto-grants-2006_08