Chloral-free DCA in oligonucleotide synthesis
A process of manufacturing oligonucleotides includes a 5′-deblocking step in which the 5-blocking group is removed with dichloroacetic acid that is essentially free of chloral. The process is useful for making oligonucleotides that are substantially free of chloral adducts.
1. A process comprising contacting an oligonucleotide bearing a dimethoxytriphenylmethyl blocking group with dichloroacetic acid having less than about 0.03 weight percent chloral hydrate.
2. The process of claim 1 , wherein said dichloroacetic acid is present in the form of a dichloroacetic acid-containing solution.
3. An oligonucleotide prepared by the process of claim 1 .
4. The oligonucleotide of claim 3 , wherein the oligonucleotide adducts of chloral are excluded to the extent that their concentration is below the limit of detection for oligonucleotide adducts of chloral.
5. The process of claim 1 , wherein the trityl blocking group is 4,4′-dimethoxytriphenylmethyl.
6. The process of claim 1 , wherein the oligonucleotide is bound to a solid support.
7. The process of claim 2 , wherein the dichloroacetic acid-containing solution further comprises an arene solvent.
8. The process of claim 7 , wherein the arene solvent is toluene.