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HRID 2270820作成日:2026年10月27日

Hydrochloric Acid → 3-(9H-fluoren-9-ylmethoxycarbonylamino)cyclohexane-1-carboxylic Acid

https://huagongshe.com/reaction/2270820

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
反応物Sodium BicarbonateHCID 516892—
反応物3-Aminocyclohexanecarboxylic acidHCID 544887—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3-(9H-fluoren-9-ylmethoxycarbonylamino)cyclohexane-1-carboxylic AcidHCID 426011057%

反応手順

3-Aminocyclohexanecarboxylic acid (10 g, 70 mmol) was added to a solution of sodium hydrogen carbonate (7.6 g, 91 mmol) in water (100 mL). A solution of 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]oxy-2,5-pyrrolidinedione (Fmoc-OSu; 28.3 g, 84 mmol) in tetrahydrofuran (200 mL) was added. The solution was stirred at room temperature overnight and then poured into 3 M HCl (200 mL). The mixture was extracted with ethyl acetate (100 mL then 50 mL) and the combined organic layers were washed with saturated brine (3×100 mL), dried (Na2SO4), filtered, and concentrated to approximately 200 mL. Crystallization occurred on concentration. The mixture was allowed to stand overnight, then the solid was filtered off, washed with ethyl acetate and dried in a vacuum oven at 55° C. to give 3-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]amino]cyclohexanecarboxylic acid (14.66, 57%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06331640B1
出典データセットuspto-grants-2001_12
ORD IDord-271c71512e8b43439ff66df919acdb3e
出典メモuspto-grants-2001_12