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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821057Generated: November 1, 2026

N-methyl-2-pyrrolidone → HCID 86057584, compound

https://huagongshe.com/reaction/1821057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantHCID 131727668HCID 131727668—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 86057584HCID 86057584—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution methyl (R/S)-(5-trifluoromethylsulfonyloxy-indan-1-yl)acetate (2.63 g, 7.80 mmol, from Step D) in N-methylpyrrolidinone (20 mL) under argon, zinc cyanide (733 mg, 6.24 mmol), Pd2 dba3 (36 mg, 39.0 μmol) and dppf (52.0 mg, 93.6 μmol) were added, and the reaction mixture was heated to 100° C. After 16 hr, the reaction mixture was concentrated iji vacuo and partitioned between EtOAc and H2O. The layers were separated and the organic layer was washed with H2O, brine and dried over MgSO4. The mixture was filtered, the filtrate concentrated in vacuo, and the residue purified by flash chromatography (5, 10% EtOAc/hexanes) on SiO2 to give 1.40 g of the title compound as a white solid: 1H NMR (CDCl3) δ 1.80-1.84 (m, 1H), 2.43-2.48 (m, 1H), 2.52 (dd, 1H, J=8.5, 15.8 Hz), 2.77 (dd, 1H, J=6.0, 15.8 Hz), 2.92-3.00 (m, 2H), 3.62-3.66 (m, 1H), 3.74 (s, 3H), 7.27 (d, 1H, J=5.5 Hz), 7.47 (d, 1H, J=7.8 Hz), 7.51 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605171B2
Source datasetuspto-grants-2009_10
ORD IDord-7615c9cc196741f7b47c4f068d7e2f59
Source noteuspto-grants-2009_10