참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 2-Isopropyl-4-isobutyl-1,3-oxazolidine | HCID 18316429 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | (2S)-4-methyl-2-(isobutylamino)pentanol | HCID 22951222 | 85.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06353006B1 |
|---|
| 출처 데이터셋 | uspto-grants-2002_03 |
|---|
| ORD ID | ord-bb64f49959e0400da318c2355a18f38a |
|---|
| 출처 메모 | uspto-grants-2002_03 |
|---|