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HRID 7891作成日:2026年10月24日

Tetramethyltin → HCID 21990863、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物TetramethyltinHCID 11661—
反応物TriphenylphosphineHCID 11776—
反応物Lithium ChlorideHCID 433294—
反応物4-Bromo-2-butyl-6-fluoro-5-methoxy-1-indanoneHCID 21990906—
触媒HCID 178418476HCID 178418476—
溶媒DimethylformamideHCID 6228—
生成物HCID 21990863HCID 2199086324.5%

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087599B2
出典データセットuspto-grants-2006_08
ORD IDord-270913168eb241f99a23be25455ccdcc
出典メモuspto-grants-2006_08