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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 600760생성일: 2026년 10월 25일

Oxalyl chloride → 3-[5-(2-Fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoyl chloride

https://huagongshe.com/reaction/600760

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참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물AtalurenHCID 11219835—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물3-[5-(2-Fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoyl chlorideHCID 5782252397%

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온도0 °C

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Compound 25 of the present invention may be prepared according to Scheme A as follows. A slurry of 3-[5-(2-fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoic acid (Compound A1, 15.0 g; 52.8 mmol) and 100 μL of dimethylformamide catalyst in 250 mL of anhydrous dichloromethane is allowed to cool to 0° C. Oxalyl chloride (9.2 mL, 105.5 mmol, 2.0 eq.) is added to this slurry over 3 minutes. The reaction mixture is then allowed to warm to room temperature, and is stirred for 16 h. The resultant yellow solution is concentrated in vacuo, azeotroped several times with anhydrous dichloromethane (2×50 mL) and dried under high vacuum for 2 hrs to give 15.5 g of 3-[5-(2-fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoyl chloride (Compound A2) as a white solid (97%): 1H NMR (CDCl3) δ 7.23-7.38 (m, 2H), 7.58-7.71 (m, 2H), 8.22-8.29 (m, 2H), 8.50 (d, J=7.8 Hz, 1H), 8.91 (t, J=1.6 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902235B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-54c0da07b7874850b1b5b825fcbc15d1
출처 메모uspto-grants-2011_03