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HRID 1921622作成日:2026年10月26日

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

https://huagongshe.com/reaction/1921622

反応式

関与物質

役割名称HCID仕込み量
反応物(4-Nitrophenyl)acetic acidHCID 4661—
反応物DimethylformamideHCID 6228—
反応物HydrazineHCID 9321—
反応物Oxalyl chlorideHCID 65578—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Nitrophenyl)acetohydrazideHCID 287331—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08173654B2
出典データセットuspto-grants-2012_05
ORD IDord-0db6b45f70844e0e9f4000e1585658c0
出典メモuspto-grants-2012_05