돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85355생성일: 2026년 10월 24일

Ethylenediamine → Benzyl N-(2-aminoethyl)carbamate

https://huagongshe.com/ko/reaction/85355

반응식

참여 물질

역할이름HCID투입량
반응물EthylenediamineHCID 3301—
반응물Methanesulfonic AcidHCID 6395—
반응물Bromocresol GreenHCID 6451—
반응물Benzyl chloroformateHCID 10387—
반응물HCID 178476685HCID 178476685—
용매EthanolHCID 702—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물Benzyl N-(2-aminoethyl)carbamateHCID 279425751%

반응 단계

Ethylenediamine (1.0 g, 16.7 mmol) is dissolved in water (3.0 mL) containing bromocresol green as an indicator. Methane sulfonic acid (2.8 g, 31 mmol) in water (3.0 mL) is added until a blue to pale yellow color transition is just achieved. The solution is diluted with ethanol (8.0 mL) and vigorously stirred. To the mixture was added the solution of Cbz-Cl (2.8 g, 16.7 mmol) in dimethoxyethane (4 mL) and 50% w/v aqueous AcOK (10 mL) at 20° C. simultaneously to maintain the pale yellow-green color of the indicator. After the additions are complete the mixture was stirred (RT, 1 h) and concentrated at low temperature under vacuum to removed the volatiles. The residue was shaken with water (20 mL) and filtered. The filtrate was then washed with toluene (3×50 mL), basified with excess 40% aqueous NaOH and extracted with toluene (3×50 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4 and evaporated to give benzyl 2-aminoethylcarbamate as an oil (1.65 g, 51%). Mass calculated for C10H14N2O2=194.23; found: [M−H]+=193.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846972B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4a860e4ef292473a9a0e191aba6087bb
출처 메모uspto-grants-2014_09