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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632221Generated: October 30, 2026

Triethylamine → HCID 86739669, compound

https://huagongshe.com/reaction/1632221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 20443609HCID 20443609—
ReactantHCID 86109706HCID 86109706—
SolventTolueneHCID 1140—
ProductHCID 86739669HCID 86739669—

Reaction Steps

4-Nitro-1-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-(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-nitro-1-anthryl) S-butyl phosphorothioate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474776
Source datasetuspto-grants-1984_10
ORD IDord-fe292ef3b89646a585265d88f3448d24
Source noteuspto-grants-1984_10