Boc-Protection / Deprotection

1-PROTECTION

The BOC (tert-butyloxycarbonyl) protecting group, chemically a di-tert-butyl dicarbonate (Boc2O), is probably the most common amine protecting group in non-peptide chemistry. The reaction conditions for the amine protection are quite flexible. The process usually achieves high yields and fast conversions under relatively mild conditions.

It is typically performed in water, water/THF, THF, or acetonitrile at room temperature or moderate heat (40°C) in the presence of a base. Dioxane and methanol have also been reported as solvents for the reaction, while an alternative common method is refluxing a biphasic mixture of chloroform and water, with NaHCO3 as a base.

Common bases for the transformation are NaOH, 4-dimethylaminopyridine (DMAP), NaHCO3.

A completely different route for the preparation of protected amines is the direct reaction of an alkyl halide with di-tert-butyl-iminodicarboxylate. Even though this is not strictly an amine protection, the method can be useful in the design of the synthetic strategy.

Reference Reaction Protocols

Prepare a solution in the solvent of choice containing the amine, 2 to 3 equivalents of BOC, and 1-1.5 equivalents of base. Stir at room temperature or moderate heat (40C). Water dilution and a subsequent extraction are typically used to isolate the product.

Examples

2-DEPROTECTION

The deprotection of a BOC-protected amine is a simple carbamate hydrolysis in acidic conditions.

The starting material is dissolved in water or organic solvent, such as toluene, dichloromethane, or ethyl acetate. Concentrated HCl, or trifluoroacetic acid (TFA) are the acids of choice. The reaction is usually fast and happens at room temperature. Biphasic systems can be used, with the protected amine dissolved in the organic phase mixed with the aqueous solution of the acid.

Other two common deprotection methods allow avoiding the use of a strong acid. They can be useful for acid-labile compounds. The trade off is a slightly more complex reaction set up and longer reaction times, up to 48-72h.

The two reagents that can be used are trimethylsilyl iodide (TMSI) and zinc bromide. The starting material is dissolved in an organic solvent, such as DCM, together with the reagent (the TMSI is usually added dropwise) and the reaction is run under stirring at room temperature for 12-24h.

Benzylation / Debenzylation

1-PROTECTION

The Benzyl (Bn) derivative is another popular amine protecting group. The N-benzylation happens by reaction of the amine with benzyl halide in the presence of a base.

Common solvents for the reaction are methanol, other primary alcohols, DMF, AcN, and some other aprotic polar organic solvents.

See “Amination of alkyl halides” section (LINK) for more details on the chemistry and reference reaction protocols.

An alternative, less common, method to introduce the protecting group on the amine is the reductive amination of benzaldehyde with sodium cyanoborohydride (NaBH3CN) in acidic conditions (HCl 6M), typically performed in methanol.

Reference Reaction Protocols

Prepare a solution of the amine in methanol or acetonitrile, add 3 equivalents of BnBr and 3 equivalents of base (typically K2CO3). Stir the reaction at reflux for 3-6h. Upon completion, quench the reaction mixture with H2O and extract the product with an appropriate organic solvent (e.g. EtOAc).

Reductive amination:

Prepare a solution of the amine in methanol or acetonitrile, add 3 equivalents of BnBr and 3 equivalents of base (typically K2CO3). Stir the reaction at reflux for 3-6h. Upon completion, quench the reaction mixture with H2O and extract the product with an appropriate organic solvent (e.g. EtOAc).

2-DEPROTECTION

The Bn protecting group is selectively cleaved by Pd-catalysed hydrogenolysis.

The reaction can be performed in numerous solvents under 1-3 bar H2 pressure and moderate heat. The catalyst of choice is 10% Pd/C. As there is no need for high hydrogen pressure, standard laboratory glassware can be used. Dedicated apparatus, such as a Parr shaker hydrogenator would certainly help, while only in certain specific situations, a dedicated autoclave is necessary.

A key element for the success of the deprotection is the choice of the right catalyst. Several different Pd/C variants are commercially available and their relative performances differ quite dramatically depending on the nature of the starting material and the reaction conditions. A 10% Pd/C with eggshell deposition is the catalysts of choice for this deprotection. Screening multiple catalysts is often necessary to identify optimal conditions for the reaction.

The handling of heterogenous Pd catalysts requires some care, as a dry catalyst can be pyrophoric, even though under normal “wet” conditions and during the reaction it is regarded as a safe and very scalable chemistry.