HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847276Generated: October 30, 2026
Water → Ethyl 5-(p-heptyloxybenzyloxy)-1-methoxy-2-indaneacetate
https://huagongshe.com/reaction/847276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-Heptyloxybenzyl chloride | HCID 14674285 | — |
| Reactant | Ethyl 5-hydroxy-1-methoxyindane-2-acetate | HCID 54284451 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 5-(p-heptyloxybenzyloxy)-1-methoxy-2-indaneacetate | HCID 53634688 | 63.8% |
Reaction Steps
In 2 ml of dimethylformamide were dissolved 190 mg of ethyl 5-hydroxy-1-methoxyindane-2-acetate and 220 mg of p-heptyloxybenzyl chloride. To the solution was added 180 mg of potassium carbonate. The mixture was stirred at 60° C. overnight. After allowing to cool, water and ethyl acetate were added to the mixture. By thoroughly shaking the mixture, the organic layer was separated. After washing with water, drying and concentrating the organic layer, the residue obtained was purified by flash chromatography (eluant: toluene/ethyl acetate (25/1)) to obtain 220 mg of ethyl 5-(p-heptyloxybenzyloxy)-1-methoxy-2-indaneacetate as a colorless oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05140046 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-56d2cfe77d024a2b87c7296f06d235e6 |
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| Source note | uspto-grants-1992_08 |
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