HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257332Generated: November 2, 2026
Chloromalonaldehyde → HCID 46785475, compound
https://huagongshe.com/reaction/1257332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromalonaldehyde | HCID 147646 | — |
| Reactant | 3-Trifluoromethylthiobenzamide | HCID 2777849 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 46785475 | HCID 46785475 | 25.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08461348B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-26f4d5995d3445e0aa39835722c95cb5 |
|---|
| Source note | uspto-grants-2013_06 |
|---|