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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632220Generated: November 3, 2026

Toluene → HCID 57245605, compound

https://huagongshe.com/reaction/1632220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 20443605HCID 20443605—
ReactantHCID 57252397HCID 57252397—
SolventEthyl AcetateHCID 8857—
ProductHCID 57245605HCID 57245605—
ProductHCID 57248772HCID 57248772—

Reaction Steps

6-Trifluoromethyl-2-anthrol (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-trifluoromethyl-2-anthryl) S-propyl phosphorothioate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474776
Source datasetuspto-grants-1984_10
ORD IDord-dade8c5aee1843afa8c4c86ccbf57aeb
Source noteuspto-grants-1984_10