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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393047생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/393047

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
반응물Sodium BicarbonateHCID 516892—
반응물3-Aminocyclohexanecarboxylic acidHCID 544887—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물3-(9H-fluoren-9-ylmethoxycarbonylamino)cyclohexane-1-carboxylic AcidHCID 426011057%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06803384B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-3fa3914117414d038e65cf407de2d41c
출처 메모uspto-grants-2004_10