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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206711Generated: November 2, 2026

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

https://huagongshe.com/reaction/2206711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenetoleHCID 7674—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-Bromo-2-chloro-3-methoxybenzoic acidHCID 71076961—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(5-Bromo-2-chloro-3-methoxyphenyl)(4-ethoxyphenyl)methanoneHCID 71076739—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371303B2
Source datasetuspto-grants-2016_06
ORD IDord-0bb5b0e10f7447aeabc2a9de5fb07cb6
Source noteuspto-grants-2016_06