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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262561Generated: November 3, 2026

Toluene → HCID 57000920, compound

https://huagongshe.com/reaction/1262561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 57252397HCID 57252397—
ReactantHCID 136094459HCID 136094459—
SolventEthyl AcetateHCID 8857—
ProductHCID 57000920HCID 57000920—
ProductHCID 57076380HCID 57076380—

Reaction Steps

3-Hydroxy-6-trifluoromethylacridine (0.01 mole), triethylamine (0.01 mole), tetrahydrofuran (25 ml) and toluene (25 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The mixture is cooled to a temperature of about 0° C. and O-(2,4-dimethylphenyl) S-propyl phosphorochloridothioate (0.01 mole) dissolved in toluene (25 ml) is added with stirring over a period of about 30 minutes. After the addition is completed the reaction mixture is allowed to warm to room temperature and stirring is continued for a period of about 16 hours. After this time the reaction mixture is filtered to remove triethylamine hydrochloride. The filtrate is then washed with water, dried over anhydrous magnesium sulfate and stripped of solvents leaving a residue. This residue is subjected to flash chromatography using ethyl acetate as the eluant to yield the desired product O-(2,4-dimethylphenyl) O-(6-trifluoromethylacridin-3-yl) S-propyl phosphorothioate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04452792
Source datasetuspto-grants-1984_06
ORD IDord-6af37582fb2f4baa8d3bd55f0ba4bd6a
Source noteuspto-grants-1984_06