Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylparaben | HCID 8434 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 14533171 | HCID 14533171 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19890431 | HCID 19890431 | 87.5% |
Reaction Steps
In a round-bottomed flask, 0.88 g of the 3-trifluoromethylheptyl p-toluenesulfonate 2, 0.4 g of ethyl p-hydroxybenzoate and 1 ml of dimethylformamide were placed, and 50 mg of sodium hydride was added thereto, followed by 8 hours of heat-refluxing and 15 hours of standing at room temperature. After the reaction, dimethylformamide was distilled off, and dilute hydrochloric acid was added to the product, which was then extracted with methylene chloride. The resultant organic layer was washed with water and dried with magnesium sulfate, followed by distilling-off of the solvent and purification by thin layer chromatography (developer: methylene chloride/ hexane=1/1) to obtain 0.7 g of ethyl p-(3-trifluoromethylheptyloxy)benzoate 3. (Yield: 80%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05073306 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-0d93dd20d3574c51ba2ff48c53d014da |
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| Source note | uspto-grants-1991_12 |
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