Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 21914489 | HCID 21914489 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21914386 | HCID 21914386 | — |
Reaction Steps
4-Bromo-3-(2-{piperidin-1-yl}ethoxy)aniline (2.99 g), 1,4-dibromobutane (1.2 ml), diisopropylethylamine (4.18 ml) and toluene (15 ml) were stirred and heated at 110° C. for 18 h. When cool, water (20 ml) was added, and the mixture was extracted with ethyl acetate (2×30 ml). The combined organic phase was washed with water, brine, dried (MgSO4) and evaporated to give the product as an orange-brown oil (2.25 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125896B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-c4dd3147fbfe43a4b2aa6e1d4fc73d5d |
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| Source note | uspto-grants-2006_10 |
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