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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13725생성일: 2026년 10월 24일

Chloroform → N-lauroyl-L-valine cyclohexylamide

https://huagongshe.com/ko/reaction/13725

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물CyclohexylamineHCID 7965—
반응물N-(1-Oxododecyl)-L-valineHCID 26658—
반응물N-Hydroxysuccinimide hydrateHCID 18987794—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물N-lauroyl-L-valine cyclohexylamideHCID 1152376444%

반응 단계

61 mg (0.20 mmol) of N-lauroyl-L-valine and 39 mg (0.26 mmol) of N-hydroxysuccinimide monohydrate were dissolved into 3.0 mL of dried chloroform. 50 mg (0.26 mmol) of 1-ethyl-3-(3-dimethylpropyl)carbodiimide hydrochloride was added thereto under argon atmosphere and in the ice bath, and stirred at 0° C. for 3 hours. 35 μL of triethylamine and 35 μL of cyclohexylamine were added thereto and stirred at room temperature overnight. Then, 20 mL of ethyl acetate was added thereto and washed with 25 mL of 0.2N hydrochloric acid, 20 mL of water and 20 mL of a saturated aqueous solution of sodium hydrogen carbonate. The mixture was then dried with anhydrous sodium sulfate and condensed under reduced pressure. The residue was purified with a thin-layer chromatography (silica gel, chloroform:methanol=20:1) to obtain 34 mg of N-lauroyl-L-valine cyclohexylamide (0.089 mmol, yield 44%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728158B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5ddb13722ece4107bca665ef961a4d5b
출처 메모uspto-grants-2010_06