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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075376Generated: November 1, 2026

Tert-butyl (2S,3S,E)-1-hydroxy-3-(4-(trifluoromethyl)phenyl)hex-4-en-2-ylcarbamate → tert-butyl (2S,3S)-1-hydroxy-3-(4-(trifluoromethyl)phenyl)hexan-2-ylcarbamate

https://huagongshe.com/reaction/2075376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl (2S,3S,E)-1-hydroxy-3-(4-(trifluoromethyl)phenyl)hex-4-en-2-ylcarbamateHCID 57633996—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-butyl (2S,3S)-1-hydroxy-3-(4-(trifluoromethyl)phenyl)hexan-2-ylcarbamateHCID 5763408898.8%

Reaction Steps

tert-Butyl (2S,3S,E)-1-hydroxy-3-(4-(trifluoromethyl)phenyl)hex-4-en-2-ylcarbamate (0.51 g, 1.4 mmol) was taken up in 10 mL of MeOH. 0.10 g of 10% Pd on carbon was added, and hydrogen was bubbled through the mixture. After 2 minutes, the bubbling ceased and the reaction was kept under a balloon of hydrogen. After 2 hours, the mixture was filtered through celite and concentrated under reduced pressure, affording tert-butyl (2S,3S)-1-hydroxy-3-(4-(trifluoromethyl)phenyl)hexan-2-ylcarbamate (0.50 g, 97% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919504B2
Source datasetuspto-grants-2011_04
ORD IDord-1b2c9c7b91e141dca832e10feb1efd21
Source noteuspto-grants-2011_04