HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461098Generated: October 30, 2026
Ethyl orthoformate → 3-Ethoxy-5-methoxy-2-methyl-1H-indene
https://huagongshe.com/reaction/461098
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 6-Methoxy-2-methyl-2,3-dihydro-1H-inden-1-one | HCID 231178 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Ethoxy-5-methoxy-2-methyl-1H-indene | HCID 21395300 | — |
Reaction Steps
6-Methoxy-2-methylindanone [1.76 g (0.01 mole)] is dissolved in 6.5 ml of absolute ethanol (containing 20% anhydrous ether). This solution is stirred with 2.4 g (0.016 mole) of triethylorthoformate and a drop of redistilled BF3C2H5OC2H5 for about 72 hours. The reaction mixture is diluted with ether poured slowly into 8.1 ml. of 5.0% sodium hydroxide solution with crushed ice with stirring. Two layers separate and the organic layer is washed with cold water until neutral followed by saturated sodium chloride solution and dried over sodium sulfate. This is then filtered and the solvent removed and the residue distilled with 1 ml of benzene solution which contains about 47.5 mg of anhydrous p-toluene sulfonic acid to obtain 2-methyl-3-ethoxy-5-methoxyindene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04061771 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-f92ac026620f45b9966bfde0bea0641c |
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| Source note | uspto-grants-1977_12 |
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