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HRID 576338作成日:2026年10月26日

Phenetole → (5-Bromo-2-chloro-3-methoxyphenyl)(4-ethoxyphenyl)methanone

https://huagongshe.com/reaction/576338

反応式

関与物質

役割名称HCID仕込み量
反応物PhenetoleHCID 7674—
反応物Oxalyl chlorideHCID 65578—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物5-Bromo-2-chloro-3-methoxybenzoic acidHCID 71076961—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物(5-Bromo-2-chloro-3-methoxyphenyl)(4-ethoxyphenyl)methanoneHCID 71076739—

反応手順

To a solution of acid 56 (4.9 g, 18.57 mmol) in CH2Cl2 (62 mL) were added oxalyl chloride (2.1 mL, 24.14 mmol) and catalytic amounts of DMF at room temperature. The mixture was stirred at room temperature for 3 hours. The mixture was evaporated in vacuo and dried under high vacuum. The crude acid chloride was dissolved with CH2Cl2 (93 mL) and cooled to 0° C. To the mixture was added phenetole (2.4 mL, 18.57 mmol) at 0° C. and stirred at 0° C. for 5 min. To the reaction mixture was added AlCl3 (2.7 g, 20.43 mmol) portionwise at 0° C. The mixture was stirred at 0° C. for 30 min, warmed up to room temperature and stirred at room temperature for 15 hours. The mixture was poured into ice-water and extracted with CH2Cl2 (100 mL×2). The combined organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The crude product 73 was dried under high vacuum and used without further purification (7.0 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09034921B2
出典データセットuspto-grants-2015_05
ORD IDord-b2b7fc3b24c249028b4d40061bc7c671
出典メモuspto-grants-2015_05