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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1982147생성일: 2026년 10월 23일

p-Nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-chloroacetate → p-Nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-[2-ethoxyethylthio(thiocarbonyl)thio]acetate

https://huagongshe.com/ko/reaction/1982147

반응식

참여 물질

역할이름HCID투입량
반응물p-Nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-chloroacetateHCID 14050378—
반응물Potassium 2-ethoxyethyl trithiocarbonateHCID 23707565—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매DichloromethaneHCID 6344—
생성물p-Nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-[2-ethoxyethylthio(thiocarbonyl)thio]acetateHCID 1368609230.9%

반응 단계

A solution of 3.58 g potassium 2-ethoxyethyl trithiocarbonate and 3.7 g benzyltriethylammonium chloride in 100 ml methylene chloride was cooled to 0° C. under a nitrogen atmosphere and a solution of 5.3 g of p-nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-chloroacetate in 50 ml methylene chloride was added dropwise. The reaction mixture was stirred for 1 hour, then washed with three 50 ml portions of water, dried over anhydrous sodium sulfate and concentrated in vacuo to an oil. (8.6 g). The crude product was chromatographed on silica gel eluting with 5% ethyl acetate in chloroform to yield 2.3 g of the title compound as an oil. The IR spectrum of a chloroform solution of the title compound had an absorption at 5.65 micron; and the NMR spectrum in deuterochloroform showed peeks at 1.2(m,6H);2.34-3.77(c,10H);4.7,4.98(m,1H); 5.26(s,2H); 6.62,6.86(s,1H); 7.43(m,2H); and 8.16(m,2H). ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04595539
출처 데이터셋uspto-grants-1986_06
ORD IDord-e9859f4cf6b64d0caad8386a8522df1b
출처 메모uspto-grants-1986_06