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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 872941생성일: 2026년 10월 25일

Ethyl bromoacetate → Ethyl (1,4,8,11-tetraazacyclotetradec-1-yl)ethanoate

https://huagongshe.com/reaction/872941

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Potassium CarbonateHCID 11430—
반응물1,4,8,11-TetraazacyclotetradecaneHCID 64964—
용매ChloroformHCID 6212—
생성물Ethyl (1,4,8,11-tetraazacyclotetradec-1-yl)ethanoateHCID 12963737—

반응 단계

In a first phase, ethyl (1,4,8,11-tetraazacyclotetradec-1-yl)ethanoate is obtained by slowly adding 6.68 g (40.0 mmol) of ethyl bromoacetate onto a solution of 40 g (200.0 mmol) of cyclam and 16 g (116 mmol) of potassium carbonate in 1 L of chloroform. The reaction mixture is maintained under stirring at room temperature for 48 h. After filtration on celite and evaporation of the solvent, the residue is taken up in petroleum ether. The excess cyclam is filtered off, the filtrate is concentrated and ethyl (1,4,8,11-tetraazacyclotetradec-1-yl)ethanoate (so-called compound 5.0) is thereby obtained, as 11.21 g of a slightly yellow oil (yield=98%) which is used without any purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08975395B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-e3de51cb07fe422a8eb5cc6ed19af054
출처 메모uspto-grants-2015_03