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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377232Generated: October 31, 2026

HCID 15123923, compound → HCID 54296116, compound

https://huagongshe.com/reaction/1377232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15123923HCID 15123923—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54296116HCID 54296116102.2%

Reaction Steps

Then, a solution of 30.0 g (0.064 mole) of 1,1-bis(4-(4-nitrobenzoyl)phenyl)methane in 1 liter of tetrahydrofuran was added dropwise for 1 hour, and stirred for 8 hours with maintaining at 3° to 5° C. At that time, hue was changed to dark purple. After the end of the reaction was confirmed by a liquid chromatography, the solution was poured in 400 milliliters of ice water, and extracted with 800 milliliters of chloroform after adding 400 milliliters of a 4N-HCl aqueous solution. Thereafter, the solution was washed with a 6N-HCl aqueous solution, an aqueous solution of sodium hydrogencarbonate, brine and water, and then removed off chloroform by a rotary evaporator. The residue was dissolved in toluene and treated with a silica gel (800 g) column, to obtain 17.1 g of 1,1-bis(4-(1-(4-nitrophenyl)butylidene)phenyl)methane as highly viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663440
Source datasetuspto-grants-1997_09
ORD IDord-7f4e28843c9f466a83ec31007f824e80
Source noteuspto-grants-1997_09