HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661174Generated: October 29, 2026
3-Fluorobenzonitrile → HCID 178513300, compound
https://huagongshe.com/reaction/1661174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluorobenzonitrile | HCID 67880 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178513300 | HCID 178513300 | 96% |
Reaction Steps
To a mixture of 3-Fluoro-benzonitrile (1.21 g, 10 mmol) and DIEA (5.20 ml, 30 mmol) in EtOH (20 ml) was added 2.08 g of Hydroxylamine hydrochloride (30 mmol) and the reaction was heated at 70° C. for 48 h. Half of the solvent was removed under reduced pressure. The mixture was poured in DCM (100 ml) and water (30 ml). 2.5 ml of NaOH 1N was added until pH=9-10. The organic layer was separated and the aqueous phase was extracted with DCM. The organics layers were combined, washed with water, dried over MgSO4, filtered and evaporated under reduced pressure to afford 1.48 g (96%) of N-Hydroxy-3-fluoro-benzamidine as a white solid which can be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030331B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-3d2014fa873b4881b9c5787bc5283598 |
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| Source note | uspto-grants-2011_10 |
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