Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Butylaniline | HCID 7694 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 4763823 | HCID 4763823 | 63% |
Reaction Steps
To a flask equipped with a magnetic stirrer, reflux condenser, and a nitrogen inlet was added 4-n-butylaniline (48.5 grams, 0.325 moles), 1-fluoro-4-nitrobenzene (15.3 grams, 0.108 moles) and anhydrous methyl sulfoxide (120 ml). The contents of the flask were heated at 100° C. for 3 days; cooled to room temperature; partitioned between diethyl ether (300 ml) and water (100 ml). The ether extract was washed with water (4×100 ml) followed by brine (2×50 ml). The ether extract was dried over anhydrous magnesium sulfate, filtered and concentrated m vacuo to yield a brown oily residue. The residue was re-crystallized from hexane (300 ml) to yield 18.4 grams of product as a yellow solid. 1H NMR (CDCl3) δ 8.1(d, 2H), 7.2(d, 2H), 7.15(d, 2H), 6.9(d, 2H), 6.3(bs, 1H), 2.6(t 2H), 1.6(pent, 2H), 1.4(hextet, 2H), 0.9(t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683017B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-39e1e7bf405641069072ab7eb7479781 |
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| Source note | uspto-grants-2010_03 |
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