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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262560Generated: November 3, 2026

Tetrahydrofuran → HCID 57323816, compound

https://huagongshe.com/reaction/1262560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 13127437HCID 13127437—
ReactantHCID 20456884HCID 20456884—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 57323816HCID 57323816—

Reaction Steps

2-Bromo-4-hydroxyacridine (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,S-diethyl phosphorochloridodithioate (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,S-diethyl O-(2-bromo-6-methylacridin-4-yl) phosphorodithioate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04452792
Source datasetuspto-grants-1984_06
ORD IDord-ba25049d18f8410b9f4f07563bce2909
Source noteuspto-grants-1984_06