Hello, new here.
I hope someone can help interpret this spectra, I would be very grateful.
Starting from α-methyl styrene and bromoform, I synthesized 1-methyl-2,2-dibromocyclopropylbenzene. Using MeLi in dry ether under N2 via a Skattebol rearrangement this turned into 1-methylpropa-1,2-dienylbenzene (allene). The remaining MeLi was quenched with water. The product was identified via proton NMR. Impurities were detected and I performed a flash column (98 hexane:1 dichloromethane:1 ethyl acetate). Same impurities were detected again. I performed a TLC plate using same solvent ratio. It produced two bands with RF=.75 and RF=.24. The first band from the bottom (.25) was trace amounts of acetophenone while the second band was the desired product. From HNMR it can be seen that the impurity remains. I performed plate once again. Same result.
I think that the allene might be being oxidized by air, this would also explain why acetophenone is also detected.
The NMR is a cryptic, from the integration values of the aromatic protons I can see that the impurity is also aromatic. But I cannot account for the rest of the peaks.
Spectra is attached. Last attachment is structure of the allene.
Doublet at 5.0ppm is CH2 from allene. Triplet at 2.1 ppm is methyl from allene.
Singlet at 5.3ppm is solvent (methylene chloride)