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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376613Generated: October 28, 2026

Tri-o-tolylphosphine → HCID 10216245, compound

https://huagongshe.com/reaction/2376613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri-o-tolylphosphineHCID 80271—
ReactantHCID 69268189HCID 69268189—
Catalystpalladium(II) acetateHCID 167845—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 10216245HCID 1021624524%

Reaction Steps

A mixture of the N-(6,7-Methylenedioxyquinolin-4-yl)-N-(butyl)-2-iodo-4,5-dimethoxybenzamide (1.0 mmol equiv.), Pd(OAc)2 (0.2 mmol equiv.), P(o-tolyl)3 (0.4 mmol equiv.), and Ag2CO3 (2.0 mmol equiv) was heated to reflux in DMF (30 mL per mmol equiv.) with stirring. The reaction mixture was allowed to cool to room temperature, diluted with CHCl3, and filtered through Celite. The sicciate was extensively washed with 10% CH3OH in CHCl3. The filtrate was concentrated in vacuo and the residue chromatographed on silica gel using chloroform:methanol to provide the title compound; (24% yield); reaction time 45 min; mp 224° C. (dec.); IR (KBr) 1654; 1H NMR (CDCl3); δ 0.99 (t, 3H, J=7.4), 1.62 (m, 2H), 2.09 (m, 2H), 4.07 (s, 3H), 4.14 (s, 3H), 4.49 (m, 2H), 6.19 (s, 2H), 7.50 (s, 1H), 7.61 (s, 1H), 7.70 (s, 1H), 7.92 (s, 1H), 9.40 (s, 1H); 13C NMR (CDCl3) δ 13.7, 20.2, 31.2, 50.6, 56.3, 56.4, 100.7, 102.0, 102.2, 107.4, 108.8, 111.7, 114.9, 119.5, 127.4, 141.1, 143.7, 147.1, 147.5, 149.8, 150.3, 154.1, 164.0; HRMS calcd for C23H22N2O5H, 406.1529; found 406.1534.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468366B2
Source datasetuspto-grants-2008_12
ORD IDord-7f75e2caec224ee88ce3191d4375010f
Source noteuspto-grants-2008_12