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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113636Generated: November 1, 2026

3,3-Dimethyl-1-butyne → HCID 59811264, compound

https://huagongshe.com/reaction/2113636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-Dimethyl-1-butyneHCID 13512—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 6-chloropyridine-3-carboxylateHCID 254249—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59811264HCID 5981126499.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

6-Chloronicotinic acid methyl ester (500 mg; 2.93 mmol) was suspended in 1,4-dioxane (3 ml) in a 5 ml reaction vial. To the vessel was added dichlorobis(triphenylphosphine)palladium(II) (70 mg; 3 mol %), copper iodide (12 mg), N,N-diisopropylethylamine (0.63 ml; 3.5 mmol) and 3,3-dimethylbut-1-yne (0.44 ml; 3.5 mmol). The vessel was sealed and the mixture was heated at 80° C. for 24 hrs. The solvents were evaporated to dryness and 20 ml of tetrahydrofuran and 20 ml of 10N NaOH was added. The mixture was stirred at room temperature for 30 minutes and the solvent was evaporated. The basic layer was acidified with concentrated HCl and extracted three times with EtOAc. The organic layers were washed with brine and dried over Na2SO4, filtered and evaporated to give the desired product as a brown powder (590 mg; 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432281B2
Source datasetuspto-grants-2008_10
ORD IDord-bb5fa4432c714d8e894f3e73bcdc5b1a
Source noteuspto-grants-2008_10