HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281081Generated: November 1, 2026
2,4-Difluoronitrobenzene → HCID 117772868, compound
https://huagongshe.com/reaction/2281081
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluoronitrobenzene | HCID 67967 | — |
| Reactant | 1-Fluoropropan-2-ol | HCID 101671 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 117772868 | HCID 117772868 | — |
Reaction Steps
0.29 g (3.77 mmol) 1-fluoro-propan-2-ol in 20 mL THF is cooled down to 0° C. 4.90 mL (1 M in THF; 4.90 mmol) LiHMDS is added drop wise. After 60 minutes of stirring at 0° C. 0.60 g (3.77 mmol) 2,4-difluoro-1-nitro-benzene is added. The mixture is stirred for 2 h. The mixture is diluted with water and EtOAc. The organic layer is washed with brine, separated, dried and evaporated giving rise to the crude 4-fluoro-2-(2-fluoro-1-methyl-ethoxy)-1-nitro-benzene. 80.0 mg palladium on charcoal (10%) and MeOH are added hydrogenated in a Parr apparatus (RT; 50 psi; 5 h). The catalyst is filtered off and the solvent is evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139577B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-07edebd22cb642198036e9ac56b0e46a |
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| Source note | uspto-grants-2015_09 |
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