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HRID 1661798作成日:2026年10月26日

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

https://huagongshe.com/reaction/1661798

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US08030305B2
出典データセットuspto-grants-2011_10
ORD IDord-f7f7132b2e5348c8a623f92f4956e1f1
出典メモuspto-grants-2011_10