I am designing a synthesis which is a variant of an existing synthesis with an important difference. so I need an alcohol protecting group that is stable to deprotection of Boc (TFA) and the deprotection of a benzyl group (H2, Pd/C) so the best bet i could find is TBDPS which according to greens protecting groups is fairly stable to acid. so would TBDPS be stable to the deprotection of Boc?
any protecting group must come of in a very mild way with biproducts that are easy to separate.