Octet

Octet / Protecting Groups

Fluorenylmethyloxycarbonyl

Fluorenylmethyloxycarbonyl (Fmoc) protects amines. Install with Fmoc-Cl, base. Remove with Piperidine (base). Removed by base (not acid). Orthogonal to Boc. Standard in solid-phase peptide synthesis.

Protecting Group details

Name

Fluorenylmethyloxycarbonyl

Abbreviation

Fmoc

Protects

Amines

Install Reagents

Fmoc-Cl, base

Remove Reagents

Piperidine (base)

Notes

Removed by base (not acid). Orthogonal to Boc. Standard in solid-phase peptide synthesis.

This is one row of the pKa · protecting groups sheet - print all 8 protecting groups on one page.

Protecting Groups

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tert-Butyldimethylsilyl

tert-Butyldimethylsilyl (TBS or TBDMS) protects alcohols. Install with TBSCl, imidazole, DMF. Remove with TBAF (tetrabutylammonium fluoride) or HF. Very common. Stable to many conditions. Removed by fluoride.

Benzyl

Benzyl (Bn) protects alcohols, carboxylic acids. Install with BnBr, NaH (for alcohols). Remove with H₂/Pd (hydrogenolysis). Stable to base and mild acid. Removed under hydrogenation.

Acetyl

Acetyl (Ac) protects alcohols, amines. Install with Ac₂O or AcCl, pyridine. Remove with NaOH/MeOH or K₂CO₃/MeOH. Forms ester (for OH) or amide (for NH₂). Removed by base hydrolysis.

Acetal

Acetal (-) protects aldehydes, ketones. Install with Diol (ethylene glycol), acid catalyst, remove H₂O. Remove with Aqueous acid (H₃O⁺). Stable to base, nucleophiles, reducing agents. Removed by acid.

tert-Butoxycarbonyl

tert-Butoxycarbonyl (Boc) protects amines. Install with Boc₂O, base. Remove with TFA (trifluoroacetic acid) or HCl. Common in peptide synthesis. Orthogonal to Fmoc.

Methyl ester

Methyl ester (-) protects carboxylic acids. Install with MeOH, H₂SO₄ (Fischer) or CH₂N₂. Remove with NaOH/H₂O (saponification) or LiOH. Simple protection. Easily hydrolyzed back to acid.

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