돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1691667생성일: 2026년 10월 26일

Pyridine → Methyl 3-chloro-4-{[(4-nitrophenoxy)carbonyl]amino}benzoate

https://huagongshe.com/reaction/1691667

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-Nitrophenyl chloroformateHCID 82129—
반응물Methyl 4-Amino-3-chlorobenzoateHCID 1515284—
용매DichloromethaneHCID 6344—
생성물Methyl 3-chloro-4-{[(4-nitrophenoxy)carbonyl]amino}benzoateHCID 5917875459.2%

반응 단계

To a solution of 5.43 g of 4-nitrophenyl chloroformate in 100 mL of dichloromethane was added 2.4 mL of pyridine under ice-cooling, and 5 g of methyl 4-amino-3-chlorobenzoate was added to the obtained mixture, followed by stirring at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and ethyl acetate was added to the residue, followed by washing with 1 M hydrochloric acid, water, a saturated aqueous sodium hydrogen carbonate solution, water, and a saturated aqueous sodium chloride solution in this order. The organic layer was dried over anhydrous sodium sulfate, and after filtration, the filtrate was concentrated under reduced pressure. The obtained solid was dissolved in 200 mL of toluene under heating, and left to be cooled to room temperature, and further cooled in an ice bath. The precipitated solid was collected by filtration, and dried under reduced pressure to obtain 5.59 g of methyl 3-chloro-4-{[(4-nitrophenoxy)carbonyl]amino}benzoate as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153658B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-6a46a0be34bb463eb4e4a66bd4d312c9
출처 메모uspto-grants-2012_04