Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20545960 | HCID 20545960 | — |
| Reactant | HCID 54069360 | HCID 54069360 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53752143 | HCID 53752143 | — |
Reaction Steps
O-Allyl O-(2-methoxyphenyl) chlorophosphate (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-trifluoromethyl-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-allyl O-(2-methoxyphenyl) O-(4-trifluoromethylindan-1-on-7-yl) phosphate.
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-0ccb599d700e462b8dea08a6c395d7e3 |
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| Source note | uspto-grants-1982_03 |
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