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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632222Generated: November 2, 2026

Tetrahydrofuran → HCID 57199963, compound

https://huagongshe.com/reaction/1632222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 20443597HCID 20443597—
ReactantHCID 57316881HCID 57316881—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 57199963HCID 57199963—

Reaction Steps

7-Nitro-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 S-(4-cyanophenyl) S-propyl 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 S-(4-cyanophenyl) O-(7-nitro-2-anthryl) S-propyl phosphorodithioate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474776
Source datasetuspto-grants-1984_10
ORD IDord-65f42072f4394fc0ac4deda0c1e16cab
Source noteuspto-grants-1984_10