HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327756Generated: October 25, 2026
Phenacyl bromide → Ethanone, 2-(acetyloxy)-1-phenyl-
https://huagongshe.com/reaction/327756
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethanone, 2-(acetyloxy)-1-phenyl- | HCID 222851 | — |
Reaction Steps
A mixture of 2-bromoacetophenone (199 g, 1.0M), acetic acid (200 mL) and acetic anhydride (30 mL) was stirred and heated to about 60° C. Anhydrous sodium acetate (100 g, 1.2M) was added and the reaction mixture was heated and stirred at about 130° C. for 6.0 hrs and then allowed to cool. To remove most of the salt, the reaction mixture was filtered through a sintered glass funnel. The acetic acid and acetic anhydride were removed from the filtrate using a rotary evaporator. A white solid was obtained upon cooling (yield--97.0 g). Mass spectroscopy supported the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05274072 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-013b7c690e714cb1b9f2dbb4d4b29262 |
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| Source note | uspto-grants-1993_12 |
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