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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57362Generated: October 27, 2026

Water → (2R,3S)-2-amino-3-(tert-butoxy)butan-1-ol

https://huagongshe.com/reaction/57362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 131736954HCID 131736954—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(2R,3S)-2-amino-3-(tert-butoxy)butan-1-olHCID 9041428587.1%

Reaction Steps

To a round bottom flask containing benzyl((2R,3S)-3-(tert-butoxy)-1-hydroxybutan-2-yl)carbamate (5.27 g, 17.8 mmol) was added MeOH (100 mL). Solution was degassed with nitrogen for 15 min at which time palladium on carbon (0.95 g, 0.89 mmol) in MeOH (5 mL) was added. A hydrogen atmosphere was then inserted. Resulting reaction mixture allowed to stir 40 min at room temperature at atmospheric pressure when water (2 mL) was added and once again a hydrogen atmosphere was inserted at atmospheric pressure and the subsequent reaction mixture allowed to stir 18 hr at room temperature. The reaction mixture was filtered through a pad of celite and concentrated to a brown oil. Oil redissolved in toluene and concentrated to afford (2R,3S)-2-amino-3-(tert-butoxy)butan-1-ol (2.5 g, 15.5 mmol, 87% yield) as a brown oil. LCMS m/z 162.1 (M+H)+, Rt 0.41 min (Mass ion only, no UV peak).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-245254501b2648ca98bbfdc18852d536
Source noteuspto-grants-2016_09