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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275918Generated: October 31, 2026

Pivalic acid → 12,12-Dimethyl-7-phenyl-10,12-dihydro-10-azaindeno[2,1-b]fluorene

https://huagongshe.com/reaction/2275918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivalic acidHCID 6417—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(biphenyl-4-yl)-9,9-dimethyl-9H-fluoren-2-amineHCID 20730584—
Catalystpalladium(II) acetateHCID 167845—
SolventDichloromethaneHCID 6344—
Product12,12-Dimethyl-7-phenyl-10,12-dihydro-10-azaindeno[2,1-b]fluoreneHCID 66797462—

Reaction Conditions

Temperature120 °C

Reaction Steps

50 ml of pivalic acid are added to 20 g of biphenyl-4-yl-(9,9-dimethyl-9H-fluoren-2-yl)amine (55.3 mmol), 1.2 g of palladium(II)acetate (5.5 mmol) and 0.8 g of potassium carbonate (5.5 mmol), and the mixture is stirred at 120° C. for 9 h. After this time, 1.2 g of palladium(II)acetate (5.5 mmol) are added, and the mixture is stirred at 120° C. for a further 9 h. 300 ml of dichloromethane and 0.1 M Na2CO3 solution are then added. The mixture is partitioned between water and dichloromethane, the aqueous phase is extracted three times with dichloromethane, and the combined organic phases are dried over Na2SO4 and evaporated in a rotary evaporator. The residue is recrystallised from toluene/heptane. The yield is 10 g (27.7 mmol, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126970B2
Source datasetuspto-grants-2015_09
ORD IDord-d483eccad8b84a3ba45ccad44cd9732d
Source noteuspto-grants-2015_09