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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261185생성일: 2026년 10월 27일

2-Amino-4-chlorophenol → ethyl 6-chloro-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate

https://huagongshe.com/reaction/261185

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4-chlorophenolHCID 7265—
반응물Carbonate IonHCID 19660—
반응물Ethyl 2,3-dibromopropionateHCID 97945—
용매AcetoneHCID 180—
용매Potassium CarbonateHCID 11430—
생성물ethyl 6-chloro-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylateHCID 3822578—

반응 단계

43.0 g of 2-amino-4-chlorophenol was dissolved in 500 ml of anhydrous acetone containing 42.0 g of anhydrous potassium carbonate. That mixture was heated to reflux temperature and 23.0 g of ethyl 2,3-dibromopropionate was added dropwise. In three additional portions each, additional ester and carbonate were added to the refluxing mixture until a total of 124 g of carbonate and 85.8 g of ester had been added. The mixture was refluxed for 21 hours. Solids were filtered from the mixture and washed with acetone. The filtrate was stripped of solvent and the residue was taken up in water. The water solution was extracted with ether. The ether extract was dried (MgSO4) and the solvent was stripped. The residue was eluted through a silica gel column using Solvent No. 3, the solvent was stripped and the residue was recrystallized from ethanol, then from ether to give ethyl 6-chloro-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate (3A), as white crystals, mp; 85.5°-86.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04164576
출처 데이터셋uspto-grants-1979_08
ORD IDord-872d3778b28b4206ba26c6e12b12cb97
출처 메모uspto-grants-1979_08