HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406902Generated: October 29, 2026
2-Hydrazinoethanol → HCID 53866285, compound
https://huagongshe.com/reaction/406902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Hydrazinoethanol | HCID 8017 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53866285 | HCID 53866285 | — |
Reaction Steps
1-Fluoro-4-nitrobenzene (7.1 g, 50 mmol) was dissolved in CH3CN (70 ml), 2-hydroxyethylhyrazine (purity: 90%, Aldrich, 5.0 g, 66 mmol) and K2CO3 (7.6 g, 55 mmol) were added thereto. The suspension thus obtained was stirred for 4 hrs with reflux. The resulting orange-colored suspension was concentrated under reduced pressure (reflux condenser, 10 torr, 40° C.) and ethylacetate (EA, 90 ml) and water (18 ml) were added thereto. The resulting mixture was stirred strongly at r.t. for 10 min. The organic layer was extracted and washed with the saturated brine (10 ml). The resulting solution was cooled to 10° C. and 48% HBr solution (3.7 ml) was added thereto dropwise with stirring. The pale yellow colored solid thus obtained was filtered off and dried under high vacuum (1 torr, 40° C.) to obtain the title compound as an intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754210B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-dfa4ec3d53d94a26a73a686b74698765 |
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| Source note | uspto-grants-2014_06 |
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