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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1661798생성일: 2026년 10월 24일

(4-Nitrophenyl)acetic acid → 2-(4-Nitrophenyl)acetohydrazide

https://huagongshe.com/ko/reaction/1661798

반응식

참여 물질

역할이름HCID투입량
반응물(4-Nitrophenyl)acetic acidHCID 4661—
반응물DimethylformamideHCID 6228—
반응물HydrazineHCID 9321—
반응물Oxalyl chlorideHCID 65578—
용매DichloromethaneHCID 6344—
생성물2-(4-Nitrophenyl)acetohydrazideHCID 287331—

반응 단계

A solution of 4-nitrophenylacetic acid (2.81 mmol) in dry dichloromethane (10 ML) was treated with a 2N solution of oxalyl chloride (3.0 mL) and DMF (0.02 mL) via syringe, and the reaction stirred at ambient temperature for 1 h. The reaction was concentrated to dryness in vacuo and the crude product was dissolved in dry dichloro-methane (20 mL), treated with anhydrous hydrazine (11.1 mmol) via syringe, and stirred at ambient temperature for 18 h. The resulting suspension was filtered, solids rinsed with dichloromethane, dissolved in MeOH/CH2Cl2, filtered, and filtrate concentrated in vacuo giving the title compound as an orange solid. 1H NMR (DMSO-d6) δ 8.17 (2H, d, J=8.8 Hz,), 7.54 (2H, d, J=8.8 Hz), 3.54 (2H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08030305B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-f7f7132b2e5348c8a623f92f4956e1f1
출처 메모uspto-grants-2011_10