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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58620생성일: 2026년 10월 24일

Oxalyl chloride → Ethyl 5-(2-fluorobenzyl)-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/ko/reaction/58620

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물Benzeneacetic acid, 2-fluoro-HCID 67979—
반응물DiisopropylethylamineHCID 81531—
반응물Ethyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Ethyl 5-(2-fluorobenzyl)-1,2,4-oxadiazole-3-carboxylateHCID 5518527114%

반응 단계

This compound was prepared according to general method 2 with 2-(2-fluorophenyl)acetic acid (1.19 g; 7.57 mmol) and oxalyl chloride (0.704 mL; 8.33 mmol) in dichloromethane (5 mL) with a few drops of DMF; and ethyl 2-amino-2-(hydroxyimino)acetate (1.0 g; 7.57 mmol) and N,N diisopropylethylamine (2.11 mL; 12.11 mmol) in dichloromethane (10 mL). The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.249 g (14%) of ethyl 5-(2-fluorobenzyl)-1,2,4-oxadiazole-3-carboxylate as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434722B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-91859965b028428eabb85df39e43d7b2
출처 메모uspto-grants-2016_09