HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679702Generated: October 30, 2026
Methyl iodide → 2,2-Dimethyl-5-methoxy-6,7-dichloro-1-indanone
https://huagongshe.com/reaction/1679702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Methyl-5-methoxy-6,7-dichloro-1-indanone | HCID 12395561 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2,2-Dimethyl-5-methoxy-6,7-dichloro-1-indanone | HCID 12395565 | — |
Reaction Steps
A stirred suspension of 2-methyl-5-methoxy-6,7-dichloro-1-indanone (12.2 g., 0.05 mole) and sodium hydride (1.43 g., 0.06 mole) in anhydrous 1,2-dimethoxyethane (500 ml.) is heated in an inert atmosphere at 80°-85° C. for 1 hour, cooled to 30° C. and treated with methyl iodide (8 ml.) The reaction mixture is refluxed for 15 minutes, then the solvent is distilled at reduced pressure. The crude product is poured into water (500 ml.), extracted into ether, washed with water and dried over magnesium sulfate. After evaporation of the ether the product is crystallized from methylcyclohexane affording 8.2 g. of 2,2-dimethyl-5-methoxy-6,7-dichloro-1-indanone which melts at 142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04081554 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-cf8901f777bb40d18d62b239cf958f34 |
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| Source note | uspto-grants-1978_03 |
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