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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41629Generated: October 29, 2026

Sodium Carbonate → HCID 58442824, compound

https://huagongshe.com/reaction/41629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 4642098—
ReactantMethyl 3-bromofuran-2-carboxylateHCID 53829030—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58442824HCID 5844282469.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Bromofuran-2-carboxylic acid methyl ester (2.0 g, 9.8 mmol, 1.0 eq.), 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester (3.1 g, 10 mmol, 1.0 eq.), THF (100 mL) and Na2CO3 (20 mL, 40 mmol, 4.0 eq.) were combined. The mixture was degassed and purged with nitrogen (3×). PdCl2(PPh3)2 (0.2 g, 0.3 mmol, 0.03 eq.) was added, and the mixture was again degassed and purged with nitrogen (3×), then heated at 80° C. overnight. The mixture was then cooled and the layers were separated. The THF layer was diluted with EtOAc (100 mL), washed with saturated aqueous NaCl (50 mL) and dried over Na2SO4. The material was filtered and applied onto a silica gel column and purified by chromatography with PE/EtOAc (50:1 to 10:1) to yield 4-(2-methoxycarbonylfuran-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester (2.1 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530663B2
Source datasetuspto-grants-2013_09
ORD IDord-e10e276399d74d5eadde4de0d485e870
Source noteuspto-grants-2013_09