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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422736Generated: October 26, 2026

1,1-Bis(propan-2-yl) 3,3-dimethoxycyclobutane-1,1-dicarboxylate → 7-Chloro-2-phenyl4-trifluoromethyl-quinoline

https://huagongshe.com/reaction/422736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Bis(propan-2-yl) 3,3-dimethoxycyclobutane-1,1-dicarboxylateHCID 4913359—
Reactant4-(3-Chloro-phenylamino)-1,1,1-trifluoro-4-phenyl-but-3-en-2-oneHCID 66676812—
Product7-Chloro-2-phenyl4-trifluoromethyl-quinolineHCID 14617612—

Reaction Steps

4-(3-Chloro-phenylamino)-1,1,1-trifluoro-4-phenyl-but-3-en-2-one (2.8 g, 0.0086 mole) and polyphosphoric acid (60 mL) in a 250 mL 3 neck round bottom flask was stirred mechanically under an atmosphere of Nitrogen at 165° C. internal temperature for 3 h. The reaction was poured over stirring ice water (600 ml). The product precipitated, and was collected by suction filtration, washed with water, and air dried overnight. The solids remaining in the Buchner funnel, and beaker from aqueous quench were rinsed into a flask concentrated in vacuo, then combined with the filtered sample and chromatographed on silica gel with 3:1 Hexanes/methylene chloride to afford the title compound as a white solid; 1H NMR (CDCl3, 400 MHz) δ 7.53-7.59 (m, 3H), 7.60-7.63 (dd, 1H, J=2.2 & J=9.1 Hz), 8.06-8.09 (dq, 1H, J=1.9 & J=9.0 Hz), 8.16-8.20 (m, 3H), 8.29 (d, 1H, J=2.1 Hz); 19F NMR δ −61.48; MS(ES+): 308.0 (100) [MH+], 310.0 (30) [M+2H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101613B2
Source datasetuspto-grants-2012_01
ORD IDord-3a1ffd14cf19489abe79a364c06dfeb1
Source noteuspto-grants-2012_01