HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291710Generated: November 1, 2026
Carbon Tetrachloride → HCID 15613883, compound
https://huagongshe.com/reaction/2291710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-(Trifluoromethyl)-1,2-oxazol-5-amine | HCID 13913996 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 15613883 | HCID 15613883 | 61.3% |
Reaction Steps
Acetic acid (7 ml) and anhydrous sodium acetate (0.57 g, 7.00 mmole) were added to 3-trifluoromethyl-5-aminoisoxazole (1.06 g, 7.00 mmole) with stirring at room temperature and a solution of chlorine in carbon tetrachloride (8.5 ml, 1 mole/1, 8.40 mmole) was then added dropwise to the mixture. After stirring for 1 hour at room temperature, the reaction mixture was poured into ice-water (70 ml) and it was adjusted to pH 10 with a solution of sodium hydroxide. It was extracted with methylene chloride. After the extract was dried with anhydrous sodium sulfate, the solvent was distilled off under reduced pressure to give a brown viscous liquid (0.80 g). This product was purified by column chromatography on silica gel to give a dark red liquid (0.54 g). It was further distilled under reduced pressure to give the title compound as a colorless liquid. Yield: 0.41 g (31.5%), b.p. 73.0°-74.5° C./4.0 mmHg. The structure of this product was confirmed with IR and NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04797492 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-62dbae24b16a40eb82c555ef65fe3e16 |
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| Source note | uspto-grants-1989_01 |
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