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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420847Generated: October 31, 2026

(2S,3R)-1-tert-Butoxycarbonyl-3-(3-hydroxypropyn-1-yl)-2-phenylpiperidin-3-ol → Z-(2S,3R)-1-tert-Butoxycarbonyl-3-(3-hydroxyprop-1-en-1-yl)-2-phenylpiperidin-3-ol

https://huagongshe.com/reaction/1420847

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,3R)-1-tert-Butoxycarbonyl-3-(3-hydroxypropyn-1-yl)-2-phenylpiperidin-3-olHCID 11301992—
CatalystPalladiumHCID 23938—
CatalystLindlars catalystHCID 131709914—
SolventEthyl AcetateHCID 8857—
ProductZ-(2S,3R)-1-tert-Butoxycarbonyl-3-(3-hydroxyprop-1-en-1-yl)-2-phenylpiperidin-3-olHCID 59038479100%

Reaction Steps

Palladium on calcium carbonate, poisoned with lead (Lindlar catalyst, 2 g) was added to a solution of (2S,3R)-1-tert-butoxycarbonyl-3-(3-hydroxypropyn-1yl)-2-phenylpiperidin-3-ol (Description 7; 32 g, 96.6 mmol) in ethyl acetate (300 mL) and the mixture was stirred under hydrogen (1 Atm.) for 4 h. The mixture was filtered and the solvent was evaporated under reduced pressure to give the title compound as an oil (32 g, 100%). 1H NMR (360 MHz, CDCl3) δ7.42 (2 H, d, J 7.6 Hz), 7.35-7.25 (3 H, m), 5.83 (1 H, d, J 12.3 Hz), 5.68 (1 H, dt, J 12.3, 6.0 Hz), 5.06 (1 H, s), 4.27 (1 H, m), 4.12 (2 H, m), 3.32 (1 H, m), 3.13 (1 H, s), 2.28 (1 H, t, J 5.9 Hz), 2.02 (1 H, m), 1.92-1.78 (3 H, m), and 1.32 (9 H, s). m/z (ES+) 334 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071927
Source datasetuspto-grants-2000_06
ORD IDord-b18b3c3aab5647fe935b852e6bbfc5c0
Source noteuspto-grants-2000_06