HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988867Generated: November 1, 2026
Hydrochloric Acid → 1-(4-Fluorophenyl)-1-hexanone
https://huagongshe.com/reaction/988867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | HCID 178445865 | HCID 178445865 | — |
| Catalyst | Ferric acetylacetonate | HCID 5483663 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Fluorophenyl)-1-hexanone | HCID 11183166 | — |
Reaction Steps
100 mL of tetrahydrofuran was placed into a four-neck round-bottom flask, then 7.92 g (0.05 mol) of 4-fluorobenzoyl chloride and 0.53 g (1.5 mmol) of tris(acetylacetone)iron (III) were added and stirred under a nitrogen atmosphere. To this solution pentylmagnesium bromide was added at a room temperature and stirred at a room temperature for 10 min. After completion of the reaction, this solution was acidified with dilute hydrochloric acid and the organic phase was extracted with diethyl ether. Further, the organic phase was neutralized with satd. sodium hydrogencarbonate solution and washed with satd. sodium chloride solution. The organic phase was dehydrated with anhydrous magnesium sulfate, then diethyl ether was evaporated by a rotary evaporator and dried by a vacuum pump to obtain crude FPHxO.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06635782B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-d4cdf826c79547caa836719aafe08e03 |
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| Source note | uspto-grants-2003_10 |
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