The 55‐amino‐acid B1‐domain of the streptococcal protein G shows a high binding affinity to IgG isolated from a wide range of mammalian species. Since the B1‐domain forms an extremely stable globular folding unit containing the major secondary structure elements and is devoid of proline residues and disulfide bridges, it is also a useful tool for protein folding and stability studies. Its small size makes this protein an ideal candidate for production by chemical synthesis, allowing incorporation of non‐natural amino acids with the possibility of assessing the influence of such residues on both the functional and structural characteristics of proteins.In this study, we enployed three successive chemical syntheses of the B1‐domain in order to define the optimal conditions of coupling and protection. The stepwise solid‐phase methodology using the tert ‐butyloxycarbonyl/benzyl strategy was used for this purpose.First, the sequence assembly difficulties were evaluated. After analyzing of the problems found during assembly, a second optimized synthesis was performed leading to formation of a synthetic B1‐domain with a higher yield; the synthetic B1‐domain was completely functional in its binding properties to IgG. Three orthogonal purification steps (gel‐permeation, reverse‐phase and ion‐exchange HPLC) were required to obtain a sample suitable for structural analysis by high‐resolution NMR. This study led to the conclusion that the synthetic B1‐domain adopts a three‐dimensional structure identical to that of the molecule obtained by recombinant techniques [Gronenborn, A. M., Filpula, D. R., Essig, N. Z., Achari, A., Whitlow, M., Wingfield, P. T. & Clore, G. M. (1991) Science 253, 657–661].To demonstrate the usefulness of the chemical approach for the specific introduction of labelled amino acids in the primary structure, fourteen α‐15N‐labelled amino acids were incorporated at selected critical positions during the third synthesis. This analog is the first in a series of molecules planned to study in detail the folding dynamics of the B1‐domain.