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Structure of 2201101-20-2
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tert-Butyl 2-bromo-3-fluorobenzylcarbamate features a bromo-fluoro-substituted benzyl scaffold with a bench-stable carbamate protecting group. This bifunctional intermediate enables direct coupling in late-stage diversification, where the bromine serves as a site for palladium-catalyzed cross-coupling and the fluorine modulates electronic properties. The tert-butyl carbamate facilitates easy deprotection under mild acidic conditions, streamlining access to functionalized anilines.
tert-Butyl 2-bromo-3-fluorobenzylcarbamate serves as a versatile building block for the synthesis of fluorinated arylamines, enabling efficient Suzuki-Miyaura and Buchwald-Hartwig coupling reactions. The ortho-bromo and meta-fluoro substituents provide complementary reactivity for sequential functionalization, while the tert-butyl carbamate group offers excellent stability and straightforward deprotection under mild acidic conditions. Its bench-stable solid form facilitates handling and purification in multi-step synthetic sequences.
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Lot numbers can be found on the outside label of a product: