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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240376Generated: October 27, 2026

Isopropanol → Tert-butyl 4-(4-cyanobenzyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/240376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantSodium CarbonateHCID 10340—
ReactantDimethylacetamideHCID 31374—
ReactantTert-butyl 4-(4-bromobenzyl)-4-hydroxypiperidine-1-carboxylateHCID 70851437—
Catalystpalladium(II) acetateHCID 167845—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(4-cyanobenzyl)-4-hydroxypiperidine-1-carboxylateHCID 70851493—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of tert-butyl 4-(4-bromobenzyl)-4-hydroxypiperidine-1-carboxylate (35 g), K4Fe(CN)6 (12 g), palladium(II)acetate (1.1 g), sodium carbonate (11 g), 2-propanol (7.5 mL) and DMA (150 mL) was stirred at 120° C. for 12 hr. The reaction mixture was allowed to cool to room temperature, diluted with dichloromethane, and filtered through celite. The filtrate was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648079B2
Source datasetuspto-grants-2014_02
ORD IDord-d29b2e20ce834ef7a14c9793330afdc9
Source noteuspto-grants-2014_02