HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710013Generated: October 28, 2026
Hydrochloric Acid → 1,1′-(Oxydi-4,1-phenylene)bis[2-bromoethanone]
https://huagongshe.com/reaction/710013
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1′-(Oxydi-4,1-phenylene)bis[2-bromoethanone] | HCID 3635569 | 67% |
Reaction Steps
Bromoacetyl chloride (2.22 ml, 22 mmol) was added dropwise during 15 min with stirring at −15° C. to a mixture of aluminum chloride (6.0 g, 44.8 mmol) in methylene dichloride (40 ml). The reaction mixture was stirred at −15° C. for an additional 3 min. Diphenyl ether (1.87 g, 11.0 mmol) was added during 30 min with stifling at −15° C. and the reaction mixture was allowed to warm to room temperature and then stirred for 3 h. It was then poured into a mixture of concentrated hydrochloric acid and crushed ice and extracted with methylene dichloride (2×50 ml). The combined organic extracts were washed with 2% aqueous sodium hydrogen carbonate and water and dried over Na2SO4. Evaporation of the solvent under reduced pressure gave desired product 50 3.03 g (67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181227B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-88b0a81a6b1e4a81b317138df1d7d354 |
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| Source note | uspto-grants-2015_11 |
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