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HRID 451768作成日:2026年10月26日

Ammonium Chloride → (S)-tert-butyl 1-cyclohexyl-3-hydroxypentan-2-ylcarbamate

https://huagongshe.com/reaction/451768

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Sodium borohydrideHCID 4311764—
反応物(S)-tert-butyl 1-cyclohexyl-3-oxopentan-2-ylcarbamateHCID 15730499—
溶媒MeOH tetrahydrofuranHCID 21899815—
生成物(S)-tert-butyl 1-cyclohexyl-3-hydroxypentan-2-ylcarbamateHCID 59201568—

反応手順

To a solution of (S)-tert-butyl 1-cyclohexyl-3-oxopentan-2-ylcarbamate in THF/MeOH (604/15 mL) at 0° C. was carefully added NaBH4 (630 mg, 16.66 mmol). After 20 min, sat. aq. NH4Cl was added to quench the reaction, and extracted with EtOAc, washed with brine, dried over Na2SO4, filtered, and concentrated to give (S)-tert-butyl 1-cyclohexyl-3-hydroxypentan-2-ylcarbamate (4.77 g, 96%, in a ratio of 40:60) as a white solid. MS ESI +ve m/z 286 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08487108B2
出典データセットuspto-grants-2013_07
ORD IDord-0db4cce6a1e04c7090574e707c3d1e2a
出典メモuspto-grants-2013_07