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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58601생성일: 2026년 10월 23일

3-Chlorophenylacetic acid → Ethyl 5-(3-chlorobenzyl)-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/ko/reaction/58601

반응식

참여 물질

역할이름HCID투입량
반응물3-Chlorophenylacetic acidHCID 15879—
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물Ethyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
용매PyridineHCID 1049—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Ethyl 5-(3-chlorobenzyl)-1,2,4-oxadiazole-3-carboxylateHCID 6337954428.1%

반응 단계

This compound was prepared according to general method 2 with (step I) 2-(3-chlorophenyl)acetic acid (0.646 g; 3.78 mmol) and oxalyl chloride (0.352 mL; 4.16 mmol) in dichloromethane (12 mL) with few drops of DMF and (step II) ethyl 2-amino-2-(hydroxyimino)acetate (0.5 g; 3.78 mmol) and N,N diisopropylethylamine (1.05 mL; 6.06 mmol) in dichloromethane (6 mL) and (step III) pyridine (18 mL). The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.283 g (28%) of ethyl 5-(3-chlorobenzyl)-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-605d83d794bc47fc93088dfaa8adf4b2
출처 메모uspto-grants-2016_09