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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1784339생성일: 2026년 10월 25일

6-Fluoro-5-Hydroxy-4-Nitro-Hexanoic Acid Methylamide → 4-Amino-6-Fluoro-5-Hydroxy-Hexanoic Acid Methylamide

https://huagongshe.com/reaction/1784339

반응식

참여 물질

역할이름HCID투입량
반응물6-Fluoro-5-Hydroxy-4-Nitro-Hexanoic Acid MethylamideHCID 86625110—
촉매NickelHCID 935—
용매MethanolHCID 887—
생성물4-Amino-6-Fluoro-5-Hydroxy-Hexanoic Acid MethylamideHCID 8662511190%

반응 단계

To a solution of 6-fluoro-5-hydroxy-4-nitro-hexanoic acid methylamide (0.325 g, 1.56 mmol) in MeOH (12 mL) was added Raney Ni (about 0.12 g), and the mixture was shaken under H2 (40-45 psi) at room temperature for 18 h. The black mixture was filtered through celite, and the celite was washed with additional MeOH (100 mL). The yellow solution was concentrated to give yellow oil (0.250 g, 90%), which was used without further purification. 1H NMR (CDCl3): 5.68 (br s, NH, 1H), 4.64-4.38 (m, 2H), 3.64-3.49 (m, 1H), 2.90-2.85 (m, 1H), 2.81 (d, J=5.10 Hz, 3H), 2.40-2.29 (m, 2H), 1.97-1.88 (m, 2H); Mass Spectra: ESI: calculated: 178.11. found: MH+ 179.18.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07504382B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-0b7d8e7f59b64f14b2c09fbad273ee7f
출처 메모uspto-grants-2009_03