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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351312Generated: November 2, 2026

4-Fluorobenzyl chloride → HCID 21098731, compound

https://huagongshe.com/reaction/1351312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzyl chlorideHCID 9602—
ReactantSodium HydroxideHCID 14798—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantHCID 86600997HCID 86600997—
SolventTetrahydrofuran ethyl acetateHCID 21939870—
ProductHCID 21098731HCID 21098731—

Reaction Steps

To a solution of 5-acetyl-2-amino-thiophene-3-sulfonic acid [2-(4-fluorophenyl)-2-hydroxy-ethyl]-methyl-amide (the compound of Preparation Example 99) (120 mg) in ethyl acetate-tetrahydrofuran (4:1) (30 mL) was added an aqueous solution (10 mL) of 2N sodium hydroxide. After stirring vigorously at room temperature, 4-fluorobenzyl-chloride (51 mg) was added. After 30 minutes, an aqueous solution (10 mL) of 2N sodium hydroxide, then 4-fluorobenzoyl-chloride (100 mg) were added, and the solution was stirred for 30 minutes. In addition, an aqueous solution (10 mL) of 2N sodium hydroxide, then 4-fluorobenzoyl-chloride (100 mg) were added. After stirring for 30 minutes, extraction was carried out by adding ethyl acetate, and the organic layer was dried with anhydrous magnesium sulfate. Purification was carried out by purification with silica gel column chromatography (hexane/ethyl acetate), and the title compound (59 mg) was obtained as yellow solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217723B2
Source datasetuspto-grants-2007_05
ORD IDord-8b22718dd42646838dc8da64441d108b
Source noteuspto-grants-2007_05