Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291710Generated: November 1, 2026

Carbon Tetrachloride → HCID 15613883, compound

https://huagongshe.com/reaction/2291710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantSodium HydroxideHCID 14798—
ReactantChlorineHCID 24526—
ReactantSodium AcetateHCID 517045—
Reactant3-(Trifluoromethyl)-1,2-oxazol-5-amineHCID 13913996—
SolventAcetic AcidHCID 176—
ProductHCID 15613883HCID 1561388361.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797492
Source datasetuspto-grants-1989_01
ORD IDord-62dbae24b16a40eb82c555ef65fe3e16
Source noteuspto-grants-1989_01