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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628237Generated: October 31, 2026

Acetonitrile → HCID 67497550, compound

https://huagongshe.com/reaction/1628237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 2-methylisonicotinateHCID 11542811—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
ProductHCID 67497550HCID 67497550100%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a 50 ml flask was added 8 ml of THF, acetonitrile (156 μl, 2.98 mmole), the mixture was cooled to −78° C. and then n-butyllithium (1191 μl, 2.98 mmole, 2.5 m in hexanes) was added. The reaction was stirred for 30 minutes at which time methyl 2-methylisonicotinate 16.1.B (150 mg, 0.99 mmoles) was added as a 2 ml THF solution. After 2 hour at −78° C., 500 μL of AcOH was added and the reaction was warmed to room temperature. The solvent was removed and the crude was purified on a silica gel column (eluting with 2% MeOH in DCM) to give 3-(2-methylpyridin-4-yl)-3-oxopropanenitrile 16.1.C as a light orange solid (170 mg 100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785468B2
Source datasetuspto-grants-2014_07
ORD IDord-514ec62b08674a93a398cd3f43097bf9
Source noteuspto-grants-2014_07