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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 365277생성일: 2026년 10월 26일

Boc4-aminomethylbicyclo-[2.2.2]octane nitrile → Boc-4-aminomethylbicyclo-[2.2.2]octane methylamine

https://huagongshe.com/reaction/365277

반응식

참여 물질

역할이름HCID투입량
반응물Boc4-aminomethylbicyclo-[2.2.2]octane nitrileHCID 69900746—
촉매Adams' catalystHCID 345198—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물Boc-4-aminomethylbicyclo-[2.2.2]octane methylamineHCID 131722017—

반응 단계

A solution of 6.75 g (25.5 mmol) of the product from step D in 200 ml of CH3OH plus 4 ml of HOAc and 2 ml of H2O was hydrogenated over 1.63 g of PtO2 in a Parr shaker at 55 psi for 22 hr. The catalyst was removed by filtration through Celite, and the filtrate was concentrated in vacuo to an oily residue, which was flushed/evaporated with CH3OH (1×) and CH2Cl2 (2×). Product began to crystallize toward the end of the evaporation, and ether (up to 300 ml) was added to complete the precipitation. The white solid was triturated and isolated by filtration and washing with ether to give, after drying in vacuo, the title compound as the acetate salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06127333
출처 데이터셋uspto-grants-2000_10
ORD IDord-b85fda91fe144eaaa5d806cb08dd4026
출처 메모uspto-grants-2000_10