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HRID 1172825作成日:2026年10月27日

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

https://huagongshe.com/reaction/1172825

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物2,2,6,6-TetramethylpiperidineHCID 13035—
反応物Ammonium ChlorideHCID 25517—
反応物(2-Chloro-6-fluoro-3-methoxyphenyl)trimethylsilaneHCID 46941339—
反応物4-(4-Chlorophenoxy)-2-propylbenzaldehydeHCID 57420143—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物[4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanolHCID 86622409—

反応条件

温度-40 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07834036B2
出典データセットuspto-grants-2010_11
ORD IDord-8ab7dbe4dfac470a9b7aa4d9fdbe6be1
出典メモuspto-grants-2010_11