![SOLVED: The reaction of 2-butylthiophene with n-butyllithium (n-BuLi), followed by quenching with N,N- dimethylformamide (DMF) , produces 5-butylthiophene-2-carbaldehyde in good yield. 1.n-BuLi; THF 2. DMF 2-butylthiophene 5-butylthiophene-2 ... SOLVED: The reaction of 2-butylthiophene with n-butyllithium (n-BuLi), followed by quenching with N,N- dimethylformamide (DMF) , produces 5-butylthiophene-2-carbaldehyde in good yield. 1.n-BuLi; THF 2. DMF 2-butylthiophene 5-butylthiophene-2 ...](https://cdn.numerade.com/ask_images/048b5b26f2e147e08f13b9b2c718a052.jpg)
SOLVED: The reaction of 2-butylthiophene with n-butyllithium (n-BuLi), followed by quenching with N,N- dimethylformamide (DMF) , produces 5-butylthiophene-2-carbaldehyde in good yield. 1.n-BuLi; THF 2. DMF 2-butylthiophene 5-butylthiophene-2 ...
![Scheme 86. Reagents: i, t-BuLi (2 equiv), Et 2 O, –78ºC; ii, TMEDA;... | Download Scientific Diagram Scheme 86. Reagents: i, t-BuLi (2 equiv), Et 2 O, –78ºC; ii, TMEDA;... | Download Scientific Diagram](https://www.researchgate.net/profile/Miguel-Yus-2/publication/229014398/figure/fig8/AS:393821901869061@1470905866262/Scheme-86-Reagents-i-t-BuLi-2-equiv-Et-2-O-78C-ii-TMEDA-iii-E-D-2-O-Me-3_Q640.jpg)
Scheme 86. Reagents: i, t-BuLi (2 equiv), Et 2 O, –78ºC; ii, TMEDA;... | Download Scientific Diagram
![NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/4aaa0691-61cb-47c0-99a9-f8aa4d87add9/anie202214106-toc-0001-m.jpg)
NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library
![Halogen−Metal Exchange in 1,2-Dibromobenzene and the Possible Intermediacy of 1,2-Dilithiobenzene | The Journal of Organic Chemistry Halogen−Metal Exchange in 1,2-Dibromobenzene and the Possible Intermediacy of 1,2-Dilithiobenzene | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo7013033/asset/images/large/jo7013033n00001.jpeg)
Halogen−Metal Exchange in 1,2-Dibromobenzene and the Possible Intermediacy of 1,2-Dilithiobenzene | The Journal of Organic Chemistry
![Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene | Journal of the American Chemical Society Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja8017187/asset/images/large/ja-2008-017187_0007.jpeg)
Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene | Journal of the American Chemical Society
![SOLVED: 23)Predict the product for each alkylation reaction below: 0 NaNH2 Chgbr 2. CHBr BuLi 2. CHzBr NaNHz NaNHz 2. CH3CHzBr 3. NaNHz PhCHzBr HS=H SOLVED: 23)Predict the product for each alkylation reaction below: 0 NaNH2 Chgbr 2. CHBr BuLi 2. CHzBr NaNHz NaNHz 2. CH3CHzBr 3. NaNHz PhCHzBr HS=H](https://cdn.numerade.com/ask_images/0fc8ceff225643f6bf50958ba32ad1a9.jpg)
SOLVED: 23)Predict the product for each alkylation reaction below: 0 NaNH2 Chgbr 2. CHBr BuLi 2. CHzBr NaNHz NaNHz 2. CH3CHzBr 3. NaNHz PhCHzBr HS=H
![Practical chemical synthesis of FICZ (1). (i) n-BuLi, THF, −70 °C. 77%.... | Download Scientific Diagram Practical chemical synthesis of FICZ (1). (i) n-BuLi, THF, −70 °C. 77%.... | Download Scientific Diagram](https://www.researchgate.net/publication/334371981/figure/fig3/AS:959518448025600@1605778433109/Practical-chemical-synthesis-of-FICZ-1-i-n-BuLi-THF-70C-77-ii-LiAlH4-THF.png)