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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368106Generated: November 2, 2026

N,N,N-Tributylbutan-1-aminium fluoride--hydrogen fluoride (1/1/2) → Benzyl 4-(3-fluoro-2-hydroxypropoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/2368106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N-Tributylbutan-1-aminium fluoride--hydrogen fluoride (1/1/2)HCID 11748636—
ReactantBenzyl 4-(oxiran-2-ylmethoxy)piperidine-1-carboxylateHCID 57517497—
ProductBenzyl 4-(3-fluoro-2-hydroxypropoxy)piperidine-1-carboxylateHCID 6744960949.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of benzyl 4-(oxiran-2-ylmethoxy)piperidine-1-carboxylate (1.81 g) and tetrabutylammonium dihydrogen trifluoride (3.74 g) was stirred at 120° C. overnight. The reaction mixture was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (960 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-023ef5c070954373bd9b5b3363bd4a00
Source noteuspto-grants-2014_04