HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244485Generated: October 31, 2026
Hydrochloric Acid → 2-(2-Fluorophenyl)ethan-1-ol
https://huagongshe.com/reaction/2244485
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Benzeneacetic acid, 2-fluoro- | HCID 67979 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Fluorophenyl)ethan-1-ol | HCID 2733296 | 88.4% |
Reaction Steps
11.4 g lithium aluminum hydride were initially introduced into 100 ml analytical grade tetrahydrofuran, the mixture was heated to the reflux temperature under a nitrogen atmosphere, 50 g 2-fluorophenylacetic acid, dissolved in 400 ml analytical grade tetrahydrofuran, were added dropwise and the reaction mixture was heated for a further two hours. For working up, 72 ml water followed by 250 ml half-concentrated hydrochloric acid (16 per cent by weight) were added dropwise, while cooling in an ice-bath. The mixture was extracted twice with 250 ml diethyl ether each time, the combined extracts were washed twice with 100 ml sodium bicarbonate solution (5 per cent by weight) each time, dried over sodium sulfate, filtered and concentrated and the residue was largely freed from solvent residues in vacuo. 40.2 g 2-(2-fluorophenyl)ethanol were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678834B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-725295ec08d04ecba7743abdeabc964a |
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| Source note | uspto-grants-2010_03 |
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