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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-Ethyl S-propyl chlorothiophosphate | HCID 11745722 | — |
| Reactant | 4-Nitro-7-hydroxyindan-1-one | HCID 20545974 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | O-ethyl S-propyl O-(4-nitroindan-1-on-7-yl) thiophosphate | HCID 53891676 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04322414 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-6c78b1f1a5564db5a7664d0432075382 |
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| Source note | uspto-grants-1982_03 |
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