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HRID 1054733作成日:2026年10月27日

Dimethylformamide → 2-(4-Bromophenoxy)acetamide

https://huagongshe.com/reaction/1054733

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物p-Bromophenoxyacetic acidHCID 74657—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Bromophenoxy)acetamideHCID 30286470%

反応手順

To a solution of (4-bromophenoxy)acetic acid (500 mg, 2.00 mmol) in dichloromethane (10 mL) and DMF (0.2 mL) was added 2 M oxalyl choride in methylene chloride (5 mL, 10 mmol). The reaction mixture was stirred at room temperature for 2 hours, and the solvent was removed under reduced pressure. Ammonium hydroxide (15 mL) was added dropwise via additional funnel. After addition, the mixture was extracted with EtOAc (3×20 mL). The combined organic layers were dried and concentrated in vacuo to give 2-(4-bromophenoxy)acetamide (350 mg, 70% yield) as a yellow solid. 1H NMR (400 MHz, CDCl3): δ 7.37-7.35 (m, 2 H), 6.81-6.79 (m, 2 H), 4.59 (s, 2 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09394285B2
出典データセットuspto-grants-2016_07
ORD IDord-55c2abcb2f684698bb235f78c63fe161
出典メモuspto-grants-2016_07