Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895972Generated: October 26, 2026

Phenylacetylene → tert-Butyl 4-(1-Fluoro-3-phenylprop-2-ynylidene)piperidine-1-carboxylate

https://huagongshe.com/reaction/1895972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantTert-butyl 4-[3-(5-cyanopyridin-3-yl)prop-2-ynylidene]piperidine-1-carboxylateHCID 25183829—
ReactantTert-butyl 4-[bromo(fluoro)methylidene]piperidine-1-carboxylateHCID 68795703—
Reactanttert-Butyl 4-(prop-2-yn-1-ylidene)piperidine-1-carboxylateHCID 86661548—
Producttert-Butyl 4-(1-Fluoro-3-phenylprop-2-ynylidene)piperidine-1-carboxylateHCID 86627338—

Reaction Steps

The title product was prepared following the procedure reported for the Compound of Example 45 but using phenylacetylene instead of instead of Compound 2b and Compound 66a instead of 5-bromonicotinonitrile. The residue coming from the usual work-up procedure was purified by flash chromatography (EtOAc—Petroleum Ether gradient from 5:95 to 10:90).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518916B2
Source datasetuspto-grants-2013_08
ORD IDord-251b94293d13405c9c9456a5730860d3
Source noteuspto-grants-2013_08