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HRID 17027作成日:2026年10月25日

(2S,3S)-4,4,4-Trifluoro-2-hydrazino-3-methyl-butan-1-ol HCl → (2S,3S)-2-Amino-4,4,4-trifluoro-3-methyl-butan-1-ol HCl

https://huagongshe.com/reaction/17027

反応式

関与物質

役割名称HCID仕込み量
反応物(2S,3S)-4,4,4-Trifluoro-2-hydrazino-3-methyl-butan-1-ol HClHCID 42632351—
触媒Adams' catalystHCID 345198—
溶媒Hydrochloric AcidHCID 313—
溶媒MethanolHCID 887—
生成物(2S,3S)-2-Amino-4,4,4-trifluoro-3-methyl-butan-1-ol HClHCID 42632353—

反応手順

(2S,3S)-4,4,4-Trifluoro-2-hydrazino-3-methyl-butan-1-ol HCl (130 g, 0.623 mole) was dissolved in 1.4 L MeOH with 60 mL concentrated HCl. The solution was hydrogenated with 10 g PtO2 at 50 psig for 12 hours. The mixture was filtered and the filter washed with 1 L MeOH. The MeOH was removed to dryness under vacuum at 30-40° C. The solid was chased with two portions of 1 L MeOH. The solid was stirred with 0.5 L MeOH for 1 hour and the NH4Cl was removed by filtration. To remove more NH4Cl, the filtrate can be concentrated to ⅔ volume and crystallized NH4Cl removed by filtration. The filtrate was concentrated to dryness and dried at 35° C. at <10 mm Hg. The hydrochloride can be purified by stirring with 20% v/v CH3CN: EtOAc removing a green coloring and removing essentially all the Pt to the 10 ppm level.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737303B2
出典データセットuspto-grants-2010_06
ORD IDord-bda13d8f298646e59afe23ec36bd6b1c
出典メモuspto-grants-2010_06