HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263615Generated: October 25, 2026
Benzene → Methyl(1-hydroxy-2-methyl-6-methoxy-indenyl)acetate
https://huagongshe.com/reaction/263615
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 6-Methoxy-2-methyl-2,3-dihydro-1H-inden-1-one | HCID 231178 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl(1-hydroxy-2-methyl-6-methoxy-indenyl)acetate | HCID 131718936 | — |
Reaction Steps
A solution of 13.4 g. of 6-methoxy-2-methylindanone and 19.3 g. of methyl bromoacetate in 45 ml. benzene is added over a period of 5 minutes to 21 g. of zinc amalgam (prepared according to Org. Syn. Coll., vol. 3) in 110 ml. benzene and 40 ml. dry ether. A few crystals of iodine are added to start the reaction, and the reaction mixture is maintained at reflux temperature (ca. 65°) with external heating. At three hour intervals, two batches of 10 g. zinc amalgam and 10 g. bromoester are added, and the mixture is then refluxed for eight hours. After addition of 30 ml. ethanol and 150 ml. of acetic acid, the mixture is poured into 700 ml. of 1:1 aqueous acetic acid. The organic layer is separated, and the aqueous layer is extracted twice with ether. The combined organic layers are washed thoroughly with water, ammonium hydroxide and water. Drying over sodium sulfate, evaporation of solvent in vacuo followed by pumping at 80° (bath temp.) (1-2 mm.) gives crude methyl(1-hydroxy-2-methyl-6-methoxy-indenyl)acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05643959 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-98c2847997d14e9399fc51afe34a057b |
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| Source note | uspto-grants-1997_07 |
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