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HRID 365277作成日:2026年10月27日

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

https://huagongshe.com/reaction/365277

反応式

関与物質

役割名称HCID仕込み量
反応物Boc4-aminomethylbicyclo-[2.2.2]octane nitrileHCID 69900746—
触媒Adams' catalystHCID 345198—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物Boc-4-aminomethylbicyclo-[2.2.2]octane methylamineHCID 131722017—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06127333
出典データセットuspto-grants-2000_10
ORD IDord-b85fda91fe144eaaa5d806cb08dd4026
出典メモuspto-grants-2000_10