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Acetone → (R)-2-fluoro-2-(3-bromophenyl)acetaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetone | HCID 180 | — |
| 反応物 | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| 反応物 | (5R)-(+)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone | HCID 11184391 | — |
| 反応物 | (3-Bromophenyl)acetaldehyde | HCID 20387554 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | (R)-2-fluoro-2-(3-bromophenyl)acetaldehyde | HCID 86611665 | — |
反応手順
A homogeneous mixture of (5R)-5-benzyl-2,2,3-trimethyl imidazolidin-4-one dichloroaccetic acid salt (97 mg, 0.4 mmol) and N-fluorobenzenesulfonimide (3.15 g, 10 mmol) in a 9:1 mixture of acetone and isopropanol at room temperature is treated with (3-bromophenyl)acetaldehyde (280 mg, 1.4 mmol), stirred for 1 h at room temperature, cooled to −78° C., diluted with ether, and filtered through a pad of celite. The filtercake is washed with additional ether. The combined filtrates are treated with methylsulfide (5 mL), washed with saturated NaHCO3 and brine, dried over MgSO4 and concentrated under reduced pressure to give (R)-2-fluro-2-(3-bromophenyl)acetaldehyde.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07423158B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-ad138f9c0f41405a9be1bd18bbb6fdde |
| 出典メモ | uspto-grants-2008_09 |