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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257332Generated: November 2, 2026

Chloromalonaldehyde → HCID 46785475, compound

https://huagongshe.com/reaction/1257332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromalonaldehydeHCID 147646—
Reactant3-TrifluoromethylthiobenzamideHCID 2777849—
SolventEthanolHCID 702—
ProductHCID 46785475HCID 4678547525.8%

Reaction Steps

To a solution of 3-(trifluoromethyl)benzenecarbothioamide (1.31 g, 6.37 mmol) in ethanol (15 mL) was added 2-chloropropane-1,3-dial (2.04 g, 19.1 mmol), and the mixture was heated under reflux overnight. The reaction mixture was extracted with ethyl acetate, washed successively with diluted aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate) to give 2-[3-(trifluoromethyl)phenyl]-1,3-thiazole-5-carbaldehyde (423 mg) as colorless crystals. The present compound was dissolved in ethanol (5 mL), sodium borohydride (91 mg, 2.47 mmol) was added under ice-cooling, and the mixture was stirred at room temperature overnight. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate, washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate) to give the title compound (334 mg, 78%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461348B2
Source datasetuspto-grants-2013_06
ORD IDord-26f4d5995d3445e0aa39835722c95cb5
Source noteuspto-grants-2013_06