Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexylamine | HCID 8102 | — |
| Reactant | 2-(3-Bromophenyl)-1,3-dioxolane | HCID 87306 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10586727 | HCID 10586727 | 94.6% |
Reaction Steps
According to the general procedure B, 2-(3-bromophenyl)-1,3-dioxolane (115 mg, 0.50 mmol) reacted with n-hexylamine (80 μl, 0.60 mmol) using 1 mol % of Pd(dba)2, 2 mol % of Ph5FcP(t-Bu)2, and sodium tert-butoxide (58 mg, 0.60 mmol) in toluene at 100° C. to give the title compound (118 mg, 94%) as a colorless oil: 1H-NMR (300 MHz, CDCl3): δ 7.19 (t, 1H, J=7.8 Hz), 6.81 (d, 1H, J=6.9 Hz), 6.74 (s, 1H), 6.61 (m, 1H), 5.77 (s, 1H), 4.13 (m, 2H), 4.03 (m, 2H), 3.55 (bs, 1H), 3.13 (t, 2H, J=6.9 and 7.2 Hz), 1.62 (m, 2H), 1.45-1.33 (m, 6H), 0.92 (t, 3H, J=6.0 and 6.9 Hz). 13C{1H}-NMR (100 MHz, CDCl3): δ 148.53, 138.85, 129.21, 115.07, 113.48, 110.31, 103.88, 65.15, 43.98, 31.58, 29.43, 26.78, 22.59, 14.01. GC/MS (EI): m/z 249 (M+). Anal. Calcd for C15H23NO2: C, 72.25; H, 9.30; N, 5.62. Found: C, 72.19; H, 9.43; N, 5.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562989B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-e7e4ce2f16044527abdc2d2a6f1e8dc4 |
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| Source note | uspto-grants-2003_05 |
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