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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891208Generated: October 31, 2026

Sodium Carbonate → HCID 68487457, compound

https://huagongshe.com/reaction/1891208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTert-butyl 4-(trifluoromethanesulfonyloxy)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 10991161—
ReactantMethyl 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 24824346—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
ProductHCID 68487457HCID 68487457—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a flask containing 1,1-dimethylethyl 4-(((trifluoromethyl)sulfonyl)oxy)-3,6-dihydropyridine-1(2H)-carboxylate (3.80 g, 11.5 mmol, prepared according to Heterocycles, 1996, 43, 2131-2138) were added the title compound from Example 3 Step A (3.80 g, 13.8 mmol) and trans-dichlorobis(triphenylphosphine)palladium (II) (804 mg, 1.15 mmol). Acetonitrile (57 mL) and sodium carbonate (28.7 mL, 1.0 M aqueous, 28.7 mmol) were added, and the resulting mixture was degassed via nitrogen sparge. The reaction mixture was stirred at 70° C. for 3 h, then was allowed to cool to ambient temperature and was poured into water. The mixture was extracted with EtOAc, and the organic phase was concentrated in vacuo. Purification by chromatography on silica gel (0 to 10% EtOAc in hexanes, then 10 to 100% EtOAc in hexanes) provided the title compound: LCMS m/z 276.0 [M-C4H9]+; 1H NMR (500 MHz, CDCl3) δ 7.89 (d, J=9.0 Hz, 1H), 7.24-7.22 (m, 2H), 6.12 (br s, 1H), 4.09 (br m, 2H), 3.88 (s, 3H), 3.65-3.62 (m, 2H), 2.61 (s, 3H), 2.52 (br m, 2H), 1.49 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507512B2
Source datasetuspto-grants-2013_08
ORD IDord-be5a0f81312748aeb626520829c75695
Source noteuspto-grants-2013_08