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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008752Generated: October 30, 2026

p-Anisoyl chloride → HCID 808296, compound

https://huagongshe.com/reaction/1008752

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
Reactant4-FluorophenolHCID 9732—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 808296HCID 808296140.3%

Reaction Conditions

Temperature55 °C

Reaction Steps

Triethylamine (6 mL) and a solution of 4.0 g of 4-methoxybenzoyl chloride (supplied from Tokyo Chemical Industry) in 40 mL of chloroform were added to a solution of 6.0 g of 4-fluorophenol (supplied from Tokyo Chemical Industry) in 60 mL of chloroform, and stirred at 55° C. for one hour. Then 100 mL of dichloromethane, 200 mL of water and 25 mL of an aqueous solution of 1 N sodium hydroxide were added to the reaction solution, and the mixture was separated into two liquid phases. The organic layer was dried on sodium sulfate anhydrate and subsequently concentrated, to yield 8.1 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973030B2
Source datasetuspto-grants-2011_07
ORD IDord-1855be5c86214de1a53c77eff014cbf8
Source noteuspto-grants-2011_07