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HRID 644951作成日:2026年10月23日

Trimethyl borate → (alphaR)-2-Bromo-5-chloro-alpha-methylbenzenemethanol

https://huagongshe.com/ja/reaction/644951

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl borateHCID 8470—
反応物2-Pyrrolidinemethanol, alpha,alpha-diphenyl-, (S)-HCID 2724899—
反応物1-(2-Bromo-5-chlorophenyl)ethanoneHCID 12486617—
溶媒TetrahydrofuranHCID 8028—
生成物(alphaR)-2-Bromo-5-chloro-alpha-methylbenzenemethanolHCID 50852803—

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07700778B2
出典データセットuspto-grants-2010_04
ORD IDord-15b34e9762014b7f966ed7ebc5d8bf02
出典メモuspto-grants-2010_04