HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461721Generated: October 29, 2026
Diethyl Ether → 1-(3-Bromo-2-methylphenyl)ethanone
https://huagongshe.com/reaction/461721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 3-Bromo-2-methylbenzonitrile | HCID 23433537 | — |
| Product | 1-(3-Bromo-2-methylphenyl)ethanone | HCID 20480131 | — |
Reaction Steps
To a stirred and refluxing Grignard-complex, previously prepared starting from 7.3 parts of magnesium, 52.6 parts of methyl iodide in 160 parts of ether, is added dropwise a solution of 19.6 parts of 3'-bromo-2'-methylbenzonitrile in 40 parts of ether. Upon completion, stirring at reflux is continued for 20 hours. The reaction mixture is cooled to 0° C and poured onto 500 parts of ice-water while stirring vigorously. The ethereal phase is separated, dried and evaporated. The residue is boiled in 60 parts of a 6N hydrochloric acid solution for 10 minutes. The separated oil is extracted with ether. The extract is washed with water, dried and evaporated. The residue is distilled, yielding 3'-bromo-2'- methylacetophenone; bp. 125°-128°C at 10 mm. pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04064132 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-1d8d53a3c75c4e68828cafd5680eb720 |
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| Source note | uspto-grants-1977_12 |
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