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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595236Generated: November 2, 2026

Sodium Acetate → (4-Chlorothiophen-2-yl)(4-fluorophenyl)methanone

https://huagongshe.com/reaction/1595236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant2-Bromo3-chloro-5-(4-fluorobenzoyl)-thiopheneHCID 21704863—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(4-Chlorothiophen-2-yl)(4-fluorophenyl)methanoneHCID 21704890—

Reaction Steps

A slurry of 5% palladium on charcoal (20 g) in ethanol (100 ml) was added under nitrogen gas to a solution of the above 2-bromo3-chloro-5-(4-fluorobenzoyl)-thiophene (299.4 9 ) in ethanol (3.400 ml), containing sodium acetate (77.0 g),and the mixture was hydrogenated for 3 hours at room temperature and pressure (total uptake of hydrogen was 22,994 ml). The reaction mixture was filtered through a dicalite pad and the pad was washed with ethanol (2×200 ml). The filtrate was taken to low volume (approximately 2 l) and added to water (17 l). The precipitate was filtered and while damp it was dissolved in dichloromethane (1 l) which was then reduced in volume to approximately 500 ml. Methanol (500 ml) was added and the remainder of the dichloromethane was removed by distillation. The resultant crystals were filtered and dried to give 4-chloro-2-(4-fluorobenzoyl)thiophene as a white solid (169 g). A second crop (19.2 g) was obtained and recrystallised from dichloromethane/methanol to give more of the purified product (12.9 g). The crops were combined and used in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288085B1
Source datasetuspto-grants-2001_09
ORD IDord-490925a5fd174cdf833e259554cad9a7
Source noteuspto-grants-2001_09