HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222851Generated: November 1, 2026
4-Benzyloxyaniline → HCID 68839626, compound
https://huagongshe.com/reaction/222851
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Benzyloxyaniline | HCID 22860 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 68839626 | HCID 68839626 | — |
Reaction Steps
To 600 μL of 2-fluoro-nitrobenzene, 6 mL of DMSO are added 1.7 g of 4-(benzyloxy)aniline (1.5 equivalents) and 1.02 g of potassium tert-butanolate (1.6 equivalents). The whole is heated to 110° C. for 1 h 30. The medium is then hydrolyzed and extracted several times with ethyl acetate. The organic phases are washed with a saturated solution of sodium chloride, dried on magnesium sulfate, filtered and then concentrated under reduced pressure. A silica gel chromatography of the residue (cyclohexane/ethyl acetate: 99/1) allows 754 mg of the desired product to be isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207373B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-9874b494d5f048909704cfb0800d8865 |
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| Source note | uspto-grants-2012_06 |
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