HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501973Generated: November 1, 2026
2-Fluoro-5-formylbenzonitrile → 2-Fluoro-5-(1-hydroxyethyl)benzonitrile
https://huagongshe.com/reaction/1501973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoro-5-formylbenzonitrile | HCID 2769582 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Fluoro-5-(1-hydroxyethyl)benzonitrile | HCID 57780028 | — |
Reaction Steps
3-Cyano-4-fluorobenzaldehyde (2.17 g, 14.7 mmol) was dissolved in THF (50 mL) then cooled to −70° C. To this mixture was added methyl magnesium bromide (5.34 mL, 16.0 mmol). The mixture was stirred for 1 h, then was quenched with brine and extracted with ether. The ethereal layer was separated, dried over Na2SO4, filtered, and evaporated to dryness. The residue was purified by MPLC chromatography through a 120 g Redi-sep column using 0-50% EtOAc/hexane eluent to yield 2-fluoro-5-(1-hydroxyethyl)benzonitrile: LC-MS: M+1=166.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206199B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-83dc94fad154466ebd47a06e3c45911d |
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| Source note | uspto-grants-2015_12 |
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