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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732257생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea

https://huagongshe.com/reaction/732257

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2,3-Dihydrothieno(3,4-b)-1,4-dioxin-2-methanolHCID 16067438—
반응물[(4'-Cyano-1,1'-biphenyl-4-yl)oxy]-butyric acidHCID 43808885—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물N,N'-DicyclohexylureaHCID 4277—

반응 단계

1.06 g of a mixture of 80% of EDT-methanol and 20% of hydroxy-PDT (corresponding to 6.19 mmol; 4.95 mmol based on the main component EDT-methanol), 1.04 g (5.04 mmol) of N,N′-dicyclohexylcarbodiimide and 0.15 g (1.22 mmol) of 4-(dimethylamino)pyridine are dissolved in 50 ml of CH2Cl2 and cooled in an ice bath. 1.42 g (5.05 mmol) of [(4′-cyano-1,1′-biphenyl-4-yl)oxy]-butyric acid (see formula) are added in small doses while stirring to the ice-cooled solution. After 1 hour, the reaction is continued at room temperature. After a further 64 hours, the colourless precipitate (N,N′-dicyclohexylurea) formed is filtered off. The clear, colourless solution is washed in succession with 2×75 ml of 1 N HCl, 2×75 ml of saturated NaHCO3 solution and 2×75 ml of NaCl solution. The clear organic phase is dried over MgSO4, the desiccant is filtered off and the solvent is removed on a rotary evaporator. This gives 2.38 g of crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585983B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-26031c00c17143a5ba637fceddad1e32
출처 메모uspto-grants-2009_09