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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530563Generated: November 3, 2026

ethyl (2S*,3R*)-2-(dibenzylamino)-3-hydroxy-4-methyl-pentanoate → ethyl (2S*,3R*)-2-amino-3-hydroxy-4-methyl-pentanoate

https://huagongshe.com/reaction/530563

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl (2S*,3R*)-2-(dibenzylamino)-3-hydroxy-4-methyl-pentanoateHCID 86700006—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Productethyl (2S*,3R*)-2-amino-3-hydroxy-4-methyl-pentanoateHCID 8670000792.9%

Reaction Steps

In a pear flask, at rt, ethyl (2S*,3R*)-2-(dibenzylamino)-3-hydroxy-4-methyl-pentanoate (1.24 g, 3.5 mmol) was dissolved in EtOH (75 mL) and passed through the H-Cube® hydrogenator flow reactor, using 10% Pd/C as catalyst [flow:1.0 mL/min; P=1.0 bar, T=70° C.]. After evaporation of the solvent, the title compound (0.57 g, quant.) was obtained as yellowish oil and used without further purification in the following step. MS (ESI) m/z: 176 [M−H]+. 1H NMR (DMSO-d6) δ 0.83 (d, J=6.72 Hz, 3H), 0.90 (d, J=6.69 Hz, 3H), 1.19 (t, J=7.10 Hz, 3H), 1.64-1.80 (m, 1H), 3.29 (dd, J=3.36, 8.06 Hz, 1H), 3.35 (d, J=3.37 Hz, 1H), 4.08 (qd, J=0.99, 7.13 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353075B2
Source datasetuspto-grants-2016_05
ORD IDord-ede1a35433f44583b60a44afa7f3164a
Source noteuspto-grants-2016_05