Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Carbazole | HCID 6854 | — |
| Product | HCID 19773852 | HCID 19773852 | — |
Reaction Steps
N-Phenylbenzaldimine (1.35 g, 0.0075 mol) and 9-benzylcarbazole (1.29 g, 0.0077 mol) were heated at 75° C. for 30 min in dimethylformamide (dry), 50 mL, and potassium tert-butoxide (0.10 g, 0.00089 mol). Based on reversed-phase HPLC results, the reaction was complete after 3 min. Aqueous work-up as above and recrystallization of the precipitate frommethanol gave needles mp 160°-2° C. (81%). 1H NMR (200 MHz, CDCl3) δ (assignment): 6.85-7.09 (m, 2H, aromatic). MS [m/e (70 eV, % of base peak)] C26H19N 345 (M+.,100), 267 (M+. -PhH, 25.8), 178 PhCCPh+., 47.5), 167 (carbazole+., 63.6). HRMS (m/z) for C26H19N (M+.) calcd. 345.1517 found 345.1513. FTIR (CDCl3): 3083, 3064, 3027, 1624, 1598, 1493, 1479, 1450, 1384, 1335, 1314, 1232 cm-1. Analysis: calcd. for C26H19N: C 90.40, H 5.54, N 4.05%; found: C 90.25, H 5.66, N 4.20%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05196606 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-c322d965c3d244f89465ce9cf7978ea3 |
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| Source note | uspto-grants-1993_03 |
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