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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059182Generated: October 27, 2026

Triethylamine → O-ethyl S-propyl O-(4-nitroindan-1-on-7-yl) thiophosphate

https://huagongshe.com/reaction/2059182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-Ethyl S-propyl chlorothiophosphateHCID 11745722—
Reactant4-Nitro-7-hydroxyindan-1-oneHCID 20545974—
SolventTolueneHCID 1140—
ProductO-ethyl S-propyl O-(4-nitroindan-1-on-7-yl) thiophosphateHCID 53891676—

Reaction Conditions

Temperature0 °C

Reaction Steps

O-Ethyl S-propyl chlorothiophosphate (0.015 mole) dissolved in dry toluene (80) is charged into a glass reaction vessel equipped with a stirrer, thermometer and gas inlet tube. The solution is cooled to about 0° C. and a solution of 4-nitro-7-hydroxyindan-1-one (0.015 mole) and triethylamine (0.0175 mole) in toluene (20 ml) is slowly added with stirring. After the addition is completed the reaction mixture is allowed to warm to room temperature and stirring is continued for a period of about 8 hours. After this time the reaction mixture is filtered and the filtrate is washed with water. The washed solution is then dried and is stripped of solvent leaving a residue. This residue is chromatographed through a 200 ml clay column using ethyl acetate and hexane mixtures as the eluant. Ten separate fractions each containing increasing percentages of ethyl acetate are collected and analyzed by IR for the product. The appropriate fractions are then combined stripped of solvent and subjected to vacuum to yield the desired product, O-ethyl S-propyl O-(4-nitroindan-1-on-7-yl) thiophosphate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04322414
Source datasetuspto-grants-1982_03
ORD IDord-6c78b1f1a5564db5a7664d0432075382
Source noteuspto-grants-1982_03