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Hexane → [4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | (2-Chloro-6-fluoro-3-methoxyphenyl)trimethylsilane | HCID 46941339 | — |
| 反応物 | 4-(4-Chlorophenoxy)-2-propylbenzaldehyde | HCID 57420143 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | [4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07834036B2 |
| 出典データセット | uspto-grants-2010_11 |
| ORD ID | ord-8ab7dbe4dfac470a9b7aa4d9fdbe6be1 |
| 出典メモ | uspto-grants-2010_11 |