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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1172825생성일: 2026년 10월 26일

Hexane → [4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanol

https://huagongshe.com/reaction/1172825

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물2,2,6,6-TetramethylpiperidineHCID 13035—
반응물Ammonium ChlorideHCID 25517—
반응물(2-Chloro-6-fluoro-3-methoxyphenyl)trimethylsilaneHCID 46941339—
반응물4-(4-Chlorophenoxy)-2-propylbenzaldehydeHCID 57420143—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물[4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanolHCID 86622409—

반응 조건

온도-40 °C

반응 단계

To a solution of 2,2,6,6-tetramethylpiperidine (2.75 g, 10 mmol) in THF (50 mL) cooled at −75° C. was added a solution of n-butyllithium in hexane (1.6 M, 6.3 mL, 10 mmol). After 15 min, 4-fluoro-2-chloro-3-(trimethylsilyl)anisole (2.3 g, 10 mmol) was added and the solution was warmed gradually to −40° C. over a 2 h period. The solution was recooled to −75° C. and a solution of the aldehyde from Step 1 of Example 3 (1.4 g, 5.0 mmol) in THF (3 mL) was added quickly. The reaction mixture was stirred for 15 min., poured into a saturated aqueous solution of ammonium chloride and extracted with ethyl acetate. After removal of the solvent, the residue was purified by chromatography on silica gel to give the title product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07834036B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-8ab7dbe4dfac470a9b7aa4d9fdbe6be1
출처 메모uspto-grants-2010_11