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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73856생성일: 2026년 10월 25일

Triethylamine → 1-[[[4-(Chloromethyl)phenyl]carbonyl]amino]cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/reaction/73856

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(Chloromethyl)benzoic acidHCID 74234—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Methyl 1-aminocyclohexane-1-carboxylate hydrochlorideHCID 22645079—
용매DichloromethaneHCID 6344—
생성물1-[[[4-(Chloromethyl)phenyl]carbonyl]amino]cyclohexanecarboxylic acid methyl esterHCID 5767285953%

반응 단계

Under ice-cooling, 9.96 g (52 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added to a solution of 8.8 g (52 mmol) of 4-(chloromethyl)benzoic acid, 10 g (52 mmol) of 1-aminocyclohexanecarboxylic acid methyl ester hydrochloride, 15 g (152 mmol) of triethylamine and 8.63 g (56 mmol) of 1-hydroxybenzotriazole in methylene chloride. After the mixture was stirred at room temperature overnight, the reaction solvent was distilled off under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate twice. The obtained organic layer was washed with a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and then saturated brine, and it was dried with anhydrous sodium sulfate. The obtained residue was purified by silica gel column chromatography to obtain 8.5 g (53%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829209B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-be8e7a24fcc54598aa5d50237ac29cc1
출처 메모uspto-grants-2014_09