HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322028Generated: October 30, 2026
2-(2-Bromophenoxy)-1-phenylethan-1-one → 7-Bromo-3-phenylbenzofuran
https://huagongshe.com/reaction/322028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(2-Bromophenoxy)-1-phenylethan-1-one | HCID 3016354 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Bromo-3-phenylbenzofuran | HCID 3016355 | 78.2% |
Reaction Steps
A mixture of 2-(2-bromophenoxy)-1-phenyl-1-ethanone (6.31 g) and polyphosphoric acid (285 g) was stirred at 95° C. for 6 h. The resulting solution was cooled to 50° C. , poured in water (2 L), extracted with Et2O (2×1 L). The combined organic extracts were washed with water (4×500 ml) and brine, dried over MgSO4 and concentrated. The residual solid was filtered on a plug of silica gel using Et2O. Recrystallization in hot hexane yielded the title compound (4.63g; 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211197B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-6cdbed8943fb48f68118e840327e7135 |
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| Source note | uspto-grants-2001_04 |
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