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HRID 1879458作成日:2026年10月26日

Chlorotrimethylsilane → HCID 15281647、化合物

https://huagongshe.com/reaction/1879458

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物(2S)-2-Amino-4,4-dimethylpentanoic acidHCID 194032—
反応物Lithium borohydrideHCID 4148881—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 15281647HCID 1528164784.2%

反応手順

To a stirred suspension of lithium borohydride (0.75 g, 34.4 mmol, 2.0 equiv.) in tetrahydrofuran (60 mL) was added trimethylsilyl chloride (7.48 g, 68.85 mmol, 4.0 equiv.) slowly over a period of 5 minutes at 0° C. under argon. To the reaction mixture was added (S)-2-amino-4,4-dimethyl-pentanoic acid (available from Chem-Impex International, Inc., Wood Dale, Ill., USA; 2.50 g, 17.2 mmol, 1.0 equiv.) in portions over a span of 10 minutes at the same temperature and the reaction was allowed to stir for 24 hours at room temperature. The reaction mixture was quenched with the slow addition of methanol (50 mL) at 0° C., and volatiles were removed by vacuum distillation. The obtained residue was treated with an aqueous solution of 20% potassium hydroxide (w/v; 10 mL) and extracted with dichloromethane (3×20 mL). The combined organic phases were dried over anhydrous sodium sulfate and concentrated under reduced pressure to give (S)-2-amino-4,4-dimethyl-pentan-1-ol (1.9 g, 84%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08314250B2
出典データセットuspto-grants-2012_11
ORD IDord-6d146d8749cf44688b1cadffb4cef64a
出典メモuspto-grants-2012_11