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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262562Generated: November 3, 2026

Triethylamine → HCID 86739444, compound

https://huagongshe.com/reaction/1262562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 86109706HCID 86109706—
ReactantHCID 136006560HCID 136006560—
SolventTolueneHCID 1140—
ProductHCID 86739444HCID 86739444—

Reaction Steps

1-Hydroxy-4-nitroacridine (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-(4-trifluoromethylphenyl) S-butyl 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-(4-trifluoromethylphenyl) O-(4-nitroacridin-1-yl) S-butyl phosphorothioate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04452792
Source datasetuspto-grants-1984_06
ORD IDord-137328f28a744ccf8ee7985646248cdc
Source noteuspto-grants-1984_06