돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12820생성일: 2026년 10월 25일

Pyridine → N-nitroso-N-(tert-butoxycarbonyl)amino-cyclopropane

https://huagongshe.com/reaction/12820

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Ethyl AcetateHCID 8857—
반응물Nitrilooxonium tetrafluoroborateHCID 11137142—
반응물tert-Butyl N-cyclopropylcarbamateHCID 15698228—
용매AcetonitrileHCID 6342—
생성물N-nitroso-N-(tert-butoxycarbonyl)amino-cyclopropaneHCID 57941319106.7%

반응 조건

온도-30 °C

반응 단계

Nitrosonium tetrafluoroborate (9.32 g, 79.8 mmol) was added carefully in several portions to a cooled (−30° C.) solution of N-(tert-butoxycarbonyl)cyclopropylamine (9.57 g, 60.9 mmol) and anhydrous pyridine (11.7 mL) in dry acetonitrile (150 mL). The solution was stirred at −30° C. for 30 minutes, and then at 0° C. for 2 hours. Ice water and EtOAc were added and the organic phase was separated and washed quickly with 1N HCl to remove pyridine. The organic phase was washed with 1N NaHCO3 and brine, dried (MgSO4), filtered, and evaporated under high vacuum with a water bath temperature below 40° C. to give N-nitroso-N-(tert-butoxycarbonyl)amino-cyclopropane (12.1 g, quantitative) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728029B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-aab3b91cf6294126a849440ff6925f04
출처 메모uspto-grants-2010_06