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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 964808생성일: 2026년 10월 26일

Isobutyrophenone → 1-(2-Methoxy-3,4,6-trimethylphenyl)-1-phenyl-2-methylpropanol

https://huagongshe.com/reaction/964808

반응식

참여 물질

역할이름HCID투입량
반응물IsobutyrophenoneHCID 69144—
반응물2-Bromo-3,5,6-trimethylanisoleHCID 21961310—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-(2-Methoxy-3,4,6-trimethylphenyl)-1-phenyl-2-methylpropanolHCID 1054211180.2%

반응 단계

A solution of 2-bromo-3,5,6-trimethylanisole (3.0 g, 13.1 mmol) in tetrahydrofuran (20 ml) was cooled to -78° C. and n-butyllithium (1.6M solution in hexane, 8.2 ml, 13.1 mmol) was added dropwise. The reaction mixture was stirred at the same temperature for 15 minutes. Then a solution of isobutyrylbenzene (1.94 g, 13.1 mmol) in tetrahydrofuran (5 ml) was added dropwise and the resulting mixture was stirred at room temperature for additional 30 minutes. The reaction mixture was diluted with water and the product was extracted with isopropyl ether. The extract was washed with water, dried and then concentrated. The residue was crystallized from hexane to obtain the desired compound (3.13 9, yield: 80.2%), m.p. 80°-81° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05770772
출처 데이터셋uspto-grants-1998_06
ORD IDord-6bb4885f6e5f42fda767c881791cc75f
출처 메모uspto-grants-1998_06