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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276260생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/276260

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물2-Isopropyl-4-isobutyl-1,3-oxazolidineHCID 18316429—
용매EthanolHCID 702—
생성물(2S)-4-methyl-2-(isobutylamino)pentanolHCID 2295122285.2%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06353006B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-bb64f49959e0400da318c2355a18f38a
출처 메모uspto-grants-2002_03