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HRID 517669作成日:2026年10月26日

Sulfuric Acid → (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine

https://huagongshe.com/reaction/517669

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Potassium BicarbonateHCID 516893—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物(2S)-5-[(benzyloxy)imino]-2-cyanopiperidineHCID 90088575—
溶媒Ethyl AcetateHCID 8857—
生成物(2S)-5-[(benzyloxy)amino]-2-cyanopiperidineHCID 11759934588%

反応条件

温度25 °C

反応手順

Sulphuric acid (11.7 ml, 0.217 mol) was slowly added to a stirred solution of (2S)-5-[(benzyloxy)imino]-2-cyanopiperidine (IX) (10 gm, 0.0436 mol, prepared according to the procedure described in step 6) in ethyl acetate (150 ml) at −10° C. After 10 minutes of stirring, sodium triacetoxy borohydride (NaHB(OOCCH3)3) (11.7 gm, 0.0519 mol, 95% purity) was added in small portions while maintaining temperature below −5° C. After completion of the addition, stirring was further continued for 2 hour at the same temperature. The pH of the reaction mixture was adjusted to about pH 7 by using 30% aqueous potassium hydrogen carbonate solution. The mixture was allowed to warm to 25° C. and the reaction mixture was filtered under suction. The organic layer was separated and the aqueous layer extracted with fresh ethyl acetate (50 ml). The combined organic layer was washed with water (50 ml) and brine (50 ml), dried over anhydrous sodium sulphate and the solvent evaporated under reduced pressure to obtain 8.88 gm of (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine (X) as an oil, in 88% yield. This was used as such for the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115131B2
出典データセットuspto-grants-2015_08
ORD IDord-11cd144b00c34a06b286f049aa7d3018
出典メモuspto-grants-2015_08