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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7846생성일: 2026년 10월 23일

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

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

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참여 물질

역할이름HCID투입량
반응물TetramethyltinHCID 11661—
반응물TriphenylphosphineHCID 11776—
반응물Lithium ChlorideHCID 433294—
반응물4-Bromo-2-butyl-5-methoxy-1-indanoneHCID 21990902—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-Butyl-5-methoxy-4-methyl-1-indanoneHCID 21990883496.7%

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-16948c22a2304cf0b6f9a96bed7293bb
출처 메모uspto-grants-2006_08