I was reflecting, and I realized I forgot something important. The rotational constant for the ground vibrational level is not the same as for the first excited vibrational level. What you would really want to do is find the rotational constant B for both vibrational levels, B0 and B1. You can find B0 by noting that R(0) and P(2) both end in the same vibrational and rotational state (v' = 1, J = 1). However, these transitions differ in the rotational level in which they begin, i.e. P(2) starts in v" = 0, J = 2 and R(0) starts in v" = 0, J = 0. Thus the energy difference between them is 6B0 and we can find B0 by noting that
6B0 = 2906.24 - 2843.62 = 62.62
B0 = 10.437 cm-1
Similarly, we find B1 by using the R(1) and P(1) transitions which start in the same ground states but finish in different rotational states. So we have
6B1 = 2925.9 - 2865.1 = 60.8
B1 = 10.133 cm-1
The rotational constants are different because B is proportional to 1/re where re is the equilibrium bond length. re shifts to the right as vibrational level increases due to anharmonicity and so as re increases, B is expected to decrease.
Now you can use the overtone equation above with the equations for any of the four transitions (with the appropriate B values) to determine the fundamental frequency and anharmonicity. For instance
2we - 6wexe = 5668
along with
we - 2wexe = 2906.24 - 2B1 = 2885.974
Sorry if anyone was confused.