関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Trimethyl borate | HCID 8470 | — |
| 反応物 | 2-Pyrrolidinemethanol, alpha,alpha-diphenyl-, (S)- | HCID 2724899 | — |
| 反応物 | 1-(2-Bromo-5-chlorophenyl)ethanone | HCID 12486617 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (alphaR)-2-Bromo-5-chloro-alpha-methylbenzenemethanol | HCID 50852803 | — |
反応手順
Trimethylborate (1.74 mL, 15.4 mmol) was added to a stirred solution of (S)-(−)-alpha,alpha-diphenyl-2-pyrrolidinemethanol (3.24 g, 12.8 mol) in tetrahydrofaran (350 mL) at room temperature. After 1.25 h, borane-methyl sulfide complex (70.4 mL of a 2M solution in tetrahydrofuran, 0.141 mol) was added slowly and a gentle effervesence was observed. The resulting soution was cooled to approximately 0° C. and a solution of 1-(2-bromo-5-chlorophenyl)ethanone (˜30.0 g, 0.128 mmol) in tetrahydrofuran (150 mL) was then added uniformly over 1 h. After the addition, the resulting mixture was allowed to warm to ambient temperature and aged overnight. The reaction mixture was concentrated under reduced pressure to approximately one quarter of its original volume, poured into 1N hydrochloric acid and extracted three times with ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo. Purification of the crude residue by flash chromatography on silica gel (9% ethyl acetate/hexanes as eluent) afforded the title compound as a colorless solid (98:2 enantiomer ratio).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07700778B2 |
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| 出典データセット | uspto-grants-2010_04 |
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| ORD ID | ord-15b34e9762014b7f966ed7ebc5d8bf02 |
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| 出典メモ | uspto-grants-2010_04 |
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