Table 2.
Use of Pol–PPh3/I2 for synthesis of amides and Weinreb amides.[a]
![]() | ||||
---|---|---|---|---|
| ||||
Entry | Acid | Amine | Time | Yield |
1 |
![]() |
![]() |
2 h | 75%[21] |
2 |
![]() |
![]() |
2 h | 72%[25] |
3 |
![]() |
![]() |
1 h | 65% |
4 |
![]() |
![]() |
11 h 3 h |
57%[20] 71%[b] |
5 |
![]() |
![]() |
6 h | 53%[41] |
6 |
![]() |
![]() |
50 min 1 h |
53%[42] 78%[b] |
7 |
![]() |
![]() |
1 h | 76%[32,c] |
8 |
![]() |
![]() |
1 h | 79%[39h,c] |
Reactions were conducted using 1 mmol each of Pol–PPh3 (2.28 mmol/g loading), I2 carboxylic acid, amine, and 1.5 mmol of iPr2NEt in 4 mL of CH2Cl2, unless specified otherwise.
Yield obtained by using 2 molar equiv each of Pol–PPh3 and I2.
2.5 Molar equiv of iPr2NEt was used.