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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262567Generated: November 2, 2026

Tetrahydrofuran → HCID 57005319, compound

https://huagongshe.com/reaction/1262567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 20456885HCID 20456885—
ReactantHCID 57296761HCID 57296761—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 57005319HCID 57005319—

Reaction Steps

2-Hydroxy-5-methylsulfinylacridine (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-fluorophenyl) S-(4-nitrophenyl) 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-fluorophenyl) O-(5-methylsulfinylacridin-2-yl) S-(4-nitrophenyl) phosphorothioate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04452792
Source datasetuspto-grants-1984_06
ORD IDord-44642b120f1d4be5b17b7406a743377a
Source noteuspto-grants-1984_06