HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244957Generated: November 3, 2026
p-Bromoacetophenone → 1,3-Propanedione, 1,3-bis(4-bromophenyl)-
https://huagongshe.com/reaction/2244957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | Ethyl 4-bromobenzoate | HCID 22043 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1,3-Propanedione, 1,3-bis(4-bromophenyl)- | HCID 147438 | — |
Reaction Steps
A mixture of ethyl-4-bromobenzoate and sodium methoxide in dry diethyl ether was stirred under an argon atmosphere After 30 min, a solution of 4′-bromoacetophenone in dry diethyl ether was then added drop-wise under stirring. The reaction mixture was stirred for 48 h under argon at room temperature. The muddy mixture was acidified and filtered under reduced pressure. The filtrate was washed with water until pH reaches about 7. The crude product was decolourized with activated charcoal and further purified by recrystallization from ethyl acetate. The white needle crystals obtained was dried in a vacuum oven at 40° C. for 24 h. Yield: 5.40 g (28.3%). M.P.: 193.2-195.4° C. The structure was confirmed by EI-MS, 1H NMR, 13C NMR, FT-IR, UV-Vis spectroscopy, and elemental analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07679082B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-05938eff83b74383af5c816ee582aaf1 |
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| Source note | uspto-grants-2010_03 |
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