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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 576338생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/576338

반응식

참여 물질

역할이름HCID투입량
반응물PhenetoleHCID 7674—
반응물Oxalyl chlorideHCID 65578—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물5-Bromo-2-chloro-3-methoxybenzoic acidHCID 71076961—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물(5-Bromo-2-chloro-3-methoxyphenyl)(4-ethoxyphenyl)methanoneHCID 71076739—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09034921B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-b2b7fc3b24c249028b4d40061bc7c671
출처 메모uspto-grants-2015_05