HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984802Generated: October 25, 2026
4-Acetyl-2-fluorobenzonitrile → 2-Fluoro-4-(2-hydroxypropan-2-yl)benzonitrile
https://huagongshe.com/reaction/984802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Acetyl-2-fluorobenzonitrile | HCID 22481653 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Fluoro-4-(2-hydroxypropan-2-yl)benzonitrile | HCID 22481626 | — |
Reaction Steps
To a stirred suspension of 4.7 g (0.019 mol) anhydrous CeCl3 in 30 mL anhydrous THF at 0° C. was added 6 mL of 3.0M CH3MgCl dropwise. Stirred at 0° C. for 45 minutes. Next a solution of 2.5 g (0.015 mol) 4-Acetyl-2-fluoro-benzonitrile in 200 mL anhydrous THF was added dropwise at 0° C. Stirred at 0° C. for 1 hour, then quenched with 2N acetic acid added dropwise. The mixture was poured into 200 mL water and acidified to pH 2 with 2N acetic acid. The aqueous layer was extracted with ethyl acetate (2×200 mL). The ethyl acetate extracts were combined, washed with water (2×40 mL), brine (1×40 mL), dried over MgSO4 and concentrated to give an oil, which was then chromatographed on silica gel eluted with 50% ethyl acetate/50% hexanes to give 1.95 g of an amber oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06869945B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-7408e970f93d4611ac1cb16dfa359160 |
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| Source note | uspto-grants-2005_03 |
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