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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514868Generated: October 31, 2026

(E)-tert-butyl 4-hydroxy-4-(4,4,4-trifluorobut-1-enyl)piperidine-1-carboxylate → (E)-4-(4,4,4-trifluorobut-1-enyl)piperidin-4-ol

https://huagongshe.com/reaction/514868

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-tert-butyl 4-hydroxy-4-(4,4,4-trifluorobut-1-enyl)piperidine-1-carboxylateHCID 90447581—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
Product(E)-4-(4,4,4-trifluorobut-1-enyl)piperidin-4-olHCID 90447571—

Reaction Steps

A solution of (E)-tert-butyl 4-hydroxy-4-(4,4,4-trifluorobut-1-enyl)piperidine-1-carboxylate (200 mg, 0.65 mmol) in 3M HCl/1,4-dioxane (5 mL) was stirred at room temperature for 2 hours. The solution was evaporated to dryness under reduced pressure to give the product which was used in the next step without further purification. LC-MS: m/z 210.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108921B2
Source datasetuspto-grants-2015_08
ORD IDord-33ba42fdad64425a9ae9196f52730cc5
Source noteuspto-grants-2015_08