Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755045Generated: October 28, 2026

Triethylamine → tert-Butyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1755045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN,N-Diethylethanamine trihydrofluorideHCID 175505—
Reactanttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
Producttert-Butyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylateHCID 2224840016%

Reaction Conditions

Temperature120 °C

Reaction Steps

1-Oxa-6-aza-spiro[2.5]octane-6-carboxylic acid tert-butyl ester (144 mg, 679 μmol), triethylamine (1.10 mL, 6.79 mmol) and triethylamine trihydrofluoride (2.85 mL, 20.4 mmol) were mixed in a sealed test tube. This mixture was stirred at 120° C. for 6.5 hours. The reaction mixture was cooled, and then quenched with a 2 N aqueous NaOH solution and extracted with ethyl acetate three times. The organic layers were combined, washed with saturated brine, dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane-AcOEt) to give 4-fluoro-4-hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (24.9 mg, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-d26de71e29c3435eb25aac5e9cb48765
Source noteuspto-grants-2015_10