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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267301Generated: October 31, 2026

Chloroacetone → HCID 11053210, compound

https://huagongshe.com/reaction/2267301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
ReactantSodium CarbonateHCID 10340—
Reactant2-Fluoro-5-nitrobenzaldehydeHCID 2734770—
ReactantSulfurHCID 5362487—
ReactantSodium hydrosulfide hydrateHCID 16211346—
Solvent1-MethylpyrrolidineHCID 8454—
ProductHCID 11053210HCID 1105321062%

Reaction Steps

A mixture of sulfur (90 mg, 2.96 mmol), sodium hydrosulfide hydrate (250 mg, 4.44 mmol) and sodium carbonate (330 mg, 2.37 mmol) in N-methylpyrrolidine (10 mL) was stirred at rt for 1 h. A solution of 2-fluoro-5-nitrobenzaldehyde (500 mg, 2.96 mmol) in N-methylpyrrolidine (2 mL) was added dropwise and the mixture was stirred at rt for 3 h. Chloroacetone (270 mg, 2.96 mmol) was added slowly with cooling and the resulting mixture was stirred at rt overnight. The reaction was quenched with 20 mL of water and sodium hydroxide (1 M) was added to adjust pH to 11. The mixture was extracted with diethyl ether (3×50 mL) and the combined organic layer was washed with brine (100 mL), dried over sodium sulfate and filtered. After removing the solvent in vacuo the product was recrystallized from methanol to give a yellow solid (400 mg, 62%). MS (M+H)+ 222.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-04484035577e48399c7774248c18c007
Source noteuspto-grants-2010_12