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HRID 276260作成日:2026年10月27日

Sodium borohydride → (2S)-4-methyl-2-(isobutylamino)pentanol

https://huagongshe.com/reaction/276260

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物2-Isopropyl-4-isobutyl-1,3-oxazolidineHCID 18316429—
溶媒EthanolHCID 702—
生成物(2S)-4-methyl-2-(isobutylamino)pentanolHCID 2295122285.2%

反応手順

To a solution of (4 g)-2-isopropyl-4-isobutyl-1,3-oxazolidine (223g, 1.3 mol) in EtOH (1.1 L) cooled to −13° C. with an ice/MeOH bath was added NaBH4 (70.3 g, 1.82 mol) in portions at such a rate that the reaction temp. did not exceed 10° C. (approximately 2 h). The reaction mixture was allowed to warm to room temp., stirred overnight, then filtered through a coarse sintered glass funnel. The resulting solids were washed with EtOH. The combined filtrate was concentrated under reduced pressure and the residue was treated with EtOAc (2 L) and water (1 L). The organic layer was dried (Na2SO4) and concentrated under reduced pressure to yield (2S)-4-methyl-2-(isobutylamino)pentan-1-ol as a viscous pale yellow oil (192 g, 85%): 1H NMR (CDCl3) δ0.90-0.96 (m, 12H), 1.18-1.24 (m, 1H), 1.32-1.39 (m, 1H), 1.58-1.72 (m, 2H), 2.33 (dd, J=11.1, 7.0 Hz, 1H), 2.49 (dd, J=11.1, 7.0 Hz, 1H), 2.61-1.67 (m, 1H), 3.19 (dd, J=10.3, 6.2 Hz, 1H), 3.60 (dd, J=10.3, 6.2 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06353006B1
出典データセットuspto-grants-2002_03
ORD IDord-bb64f49959e0400da318c2355a18f38a
出典メモuspto-grants-2002_03