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HRID 338390作成日:2026年10月26日

Dimethylformamide → 2-(4-Bromophenoxy)acetamide

https://huagongshe.com/reaction/338390

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 2M oxalyl chloride 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, 2H), 6.81-6.79 (m, 2H), 4.59 (s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889730B2
出典データセットuspto-grants-2014_11
ORD IDord-0d40f7466eff4c9ca72219133632cc17
出典メモuspto-grants-2014_11