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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892821Generated: October 26, 2026

Isobutyramide → Tert-butyl 5-cyanonicotinate

https://huagongshe.com/reaction/1892821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyramideHCID 68424—
Reactant5-Bromonicotinic acidHCID 88707—
Reactanttert-Butyl 5-bromonicotinateHCID 18422124—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystZincHCID 23994—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystHCID 15826098HCID 15826098—
ProductTert-butyl 5-cyanonicotinateHCID 29921637—

Reaction Conditions

Temperature120 °C

Reaction Steps

Instead of the starting material of Reference Example 56, that is, the compound S55, the 5-bromonicotinic acid was used for the similar procedure as in Reference Example 56. To the obtained tert-butyl 5-bromonicotinate (22.4 g), dimethylacetoamide (112 ml), tris(dibenzylideneacetone)dipalladium (1.59 g), zinc cyanide (6.1 g), diphenylphosphinoferrocene (1.92 g), and zinc powder (0.68 g) were added and the mixture was stirred under argon atmosphere at 120° C. for 1.5 hours. The reaction solution was filtered by sellite, which was then washed with ethyl acetate, and the filtrate was washed with saturated saline. The organic layer was dried over with anhydrous sodium sulfate, then concentrated. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=3/1) to obtain tert-butyl 5-cyanonicotinate (13.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507714B2
Source datasetuspto-grants-2013_08
ORD IDord-98518086b4094621b4767f148517a618
Source noteuspto-grants-2013_08