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HRID 7846作成日:2026年10月24日

Tetramethyltin → 2-Butyl-5-methoxy-4-methyl-1-indanone

https://huagongshe.com/ja/reaction/7846

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-5-methoxy-1-indanoneHCID 21990902—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-Butyl-5-methoxy-4-methyl-1-indanoneHCID 21990883496.7%

反応条件

温度100 °C

反応手順

A solution of 4-bromo-2-butyl-5-methoxy-1-indanone (1.159 g, 3.90 mmol) in anhydrous dimethylformamide (39 mL) was treated with LiCl (455 mg, 10.73 mmol), PPh3 (205 mg, 0.78 mmol), PdCl2(PPh3)2 (205 mg, 0.292 mmol) and Me4Sn (1.08 mL, 7.80 mmol). The mixture was placed under a nitrogen atmosphere, then stirred and heated in an oil bath at 100° C. for 16.5 hours. After cooling to room temperature, the mixture was diluted with water (100 mL) and extracted with Et2O (100 mL, 2×25 mL). The ether extracts were washed with brine, dried over MgSO4, filtered and evaporated under vacuum to a yellow solid (1.29 g). This material was purified by chromatography on EM silica gel 60 (230-400 mesh, 130 mL dry, packed under CH2Cl2), using CH2Cl2 as eluting solvent, to afford a 92:3:5 mixture (0.90 g) of 2-butyl-5-methoxy-4-methyl-1-indanone, the 6-methyl isomer, and the desmethyl product. This material was used as is in the next step.

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-16948c22a2304cf0b6f9a96bed7293bb
出典メモuspto-grants-2006_08