HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436371Generated: October 26, 2026
Hydrochloric Acid → 1-Propanone, 2,2-dimethyl-1-(4-phenoxyphenyl)-
https://huagongshe.com/reaction/436371
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | 4-Bromodiphenyl Ether | HCID 7565 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Propanone, 2,2-dimethyl-1-(4-phenoxyphenyl)- | HCID 41633 | — |
Reaction Steps
To a flask containing 33.6 g. of magnesium and a few crystals of iodine, is added 50 to 70 ml. of a solution of 300 g. of 4-bromodiphenyl ether in 500 ml. of absolute tetrahydrofuran. The remainder of the solution is added as needed to maintain a gentle reflux and the resulting mixture heated to reflux for 30 minutes. The resulting mixture is then added to a solution of trimethylacetyl chloride in 500 ml. of absolute tetrahydrofuran at a rate so as to maintain a temperature of from 40° to 50° C. The resulting mixture is then stirred at ambient temperture for 1 hour. 200 ml. of 2N. hydrochloric acid is then added. The organic layer is washed twice with one liter of 2N. sodium carbonate solution, dried and evaporated in vacuo to a liquid. The liquid thus obtained is distilled under reduced pressure to obtain p-phenoxypivalophenone, b.p. 136° -139° C. at 0.1 mm/Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04008327 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-214717a6e1884ed698d16f5629178edb |
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| Source note | uspto-grants-1977_02 |
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