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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602520Generated: November 1, 2026

4-Chlorophenylacetyl chloride → HCID 10094749, compound

https://huagongshe.com/reaction/602520

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophenylacetyl chlorideHCID 90692—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67267820HCID 67267820—
SolventAcetonitrileHCID 6342—
ProductHCID 10094749HCID 1009474916.5%

Reaction Conditions

Temperature150 °C

Reaction Steps

2-Chloro-N(4)-(5-chloro-thiophen-2-ylmethyl)-N(4)-methyl-benzene-1,4-diamine (100 mg) was added to a solution of 4-chlorophenylacetyl chloride (69 mg) in dry acetonitrile (2 mL) in a rubber-capped glass vial. The reaction mixture was heated in a microwave device to 150° C. for 15 minutes. The reaction mixture was poured into saturated aqueous sodium bicarbonate (5 mL) and extracted with ethyl acetate (5 mL). The organic phase was washed with water (5 mL) and brine (5 mL), dried over sodium sulfate, filtered, and evaporated to dryness. The crude product was purified by flash chromatography (heptane/ethyl acetate, gradient) to furnish 25.2 mg title compound. Yield: 16%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906537B2
Source datasetuspto-grants-2011_03
ORD IDord-0f40389350ba4282a028e4fee81e1067
Source noteuspto-grants-2011_03