HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789956Generated: October 30, 2026
Phenol → 4-Chloro-1-(2-hydroxyphenyl)butan-1-one
https://huagongshe.com/reaction/1789956
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 3-Fluorophenol | HCID 9743 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Product | 4-Chloro-1-(2-hydroxyphenyl)butan-1-one | HCID 10867311 | — |
| Product | 4-Chloro-1-(4-fluoro-2-hydroxyphenyl)butan-1-one | HCID 14773873 | — |
Reaction Steps
To a cold boron trifluoride etherate (280 mmol) solution was added 3-fluorophenol or phenol (89 mmol) and 4-chlorobutyryl chloride (178 mmol). The resulting solution was stirred at 130° C. for 18 hours. The reaction mixture was cooled and poured into ice water (100 mL). After stirring for 10 minutes, the water mixture was extracted with ether (3×100 mL). The ether layer was washed with brine (100 mL), dried over MgSO4, filtered and concentrated to a residue to afford 4-chloro-1-(4-fluoro-2-hydroxyphenyl)butan-1-one and 4-chloro-1-(2-hydroxyphenyl)butan-1-one in 52%–67% yield, which was used in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071186B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-1904c867b1b84d10aefb06cd7dec1eac |
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| Source note | uspto-grants-2006_07 |
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