Table 2.
Synthesis of formanilides in [ChCl][ZnCl2]2 as a solvent/catalyst system.
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|---|---|---|---|---|---|
| Substrate | Substrate | Product | Time (h) | Yielda (%) | M.p. °C (Lit) |
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4 | 88 |
105 (103–105)84 |
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3.5 | 72 |
126 (121–122)85 |
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3.5 | 89 |
51 (50–52)86 |
|
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3.5 | 85 |
76 (73–77)87 |
|
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4 | 83 |
156–157 (155–157)88 |
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4 | 68 |
138 (135–137)88 |
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4.15 | 66 |
177 (175–177)89 |
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4.45 | 72 | 179 |
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3.5 | 91 |
53 (48–51)90 |
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4 | 74 |
79 (78.8–79.8)91 |
|
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3.5 | 81 |
55 (51–53)92 |
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4 | 68 |
135 (129–132)92 |
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4 | 87 |
186 (182–187)93 |
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8 | < 5 | – |
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10 | NRb | – |
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10 | NRb | – | |
Reaction conditions: Aniline derivatives (1.0 mmol), formamide (1.0 mmol) and 3 mL of [ChCl][ZnCl2]2.
aIsolated yield.
bNo reaction.












































