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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853694Generated: October 30, 2026

1,1'-(Diazomethylene)bis(benzene) → HCID 58928752, compound

https://huagongshe.com/reaction/853694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(Diazomethylene)bis(benzene)HCID 61230—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant6,7-Dimethyl 5-methoxy-8-[[tris(1-methylethyl)silyl]oxy]-6,7-quinolinedicarboxylateHCID 58929007—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58928752HCID 5892875292%

Reaction Steps

A 1M solution of TBAF in THF (4 ml) was added to 5-methoxy-8-triisopropylsilanyloxy-quinoline-6,7-dicarboxylic acid dimethyl ester (0.85 g, 1.9 mmol) in 20 ml dry THF. The reaction was stirred at rt for 1 h, at which time the reaction mixture was concentrated and the residue dissolved in 100 mL diethyl ether and washed with 25 mL 1N HCl, followed by 25 mL of saturated aq. NaCl. The organic layer was concentrated and the residue was dissolved in 40 mL dichloroethane. Diphenyldiazomethane (0.7 g, 3.8 mmol) was added and the reaction temperature was raised to 70° C. for 24 h. The reaction mixture was concentrated and the residue chromatographed on silica gel (1/1 hexanes/EtOAc) to give 8-benzhydryloxy-5-methoxy-quinoline-6,7-dicarboxylic acid dimethyl ester (0.8 g, 61% yield overall). 1H NMR (CDCl3) δ 8.85 (d, 1H), 8.45 (d, 1H), 7.45 (dd, 1H), 3.98 (s, 3H), 3.85 (s, 3H), 3.74 (s, 3H); MS: 480 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253180B2
Source datasetuspto-grants-2007_08
ORD IDord-9d1649460adc40c99dc5f65bf34be258
Source noteuspto-grants-2007_08