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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 862183생성일: 2026년 10월 24일

Pyridine → Chloro-oxo-acetic acid 2-oxo-3-phenyl-2,3-dihydro-benzofuran-5-yl ester

https://huagongshe.com/ko/reaction/862183

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Oxalyl chlorideHCID 65578—
반응물5-hydroxy-3-phenyl-3H-benzofuran-2-oneHCID 10632983—
용매DichloromethaneHCID 6344—
생성물Chloro-oxo-acetic acid 2-oxo-3-phenyl-2,3-dihydro-benzofuran-5-yl esterHCID 53805502—

반응 단계

Oxalyl chloride (17.5 parts) and pyridine (0.5 parts) were added to a suspension of 5-hydroxy-2-oxo-3-phenyl-2,3-dihydrobenzfuran (22.6 parts) in dichloromethane (200 parts). After six hours reflux, chloro-oxo-acetic acid 2-oxo-3-phenyl-2,3-dihydro-benzofuran-5-yl ester was isolated and phenol (9.9 parts) added and the mixture refluxed for eighteen hours. Removal of the solvent gave the crude product oxalic acid (2-oxo-3-phenyl-2,3-dihydro-benzofuran-5-yl)ester phenyl ester (33.3 parts; 89%). Trituration in methanol and recrystallisation from ethyl acetate gave a pure product. Analysis C,70.4; H,3.7; C22H13O6 requires C,70.8; H,3.5%. M.pt.134° C., 1H and 13Cnmr gave spectra consistent with structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05717112
출처 데이터셋uspto-grants-1998_02
ORD IDord-10e38c50e6ae4d66991d36173a8c2caa
출처 메모uspto-grants-1998_02