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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304994Generated: October 25, 2026

Decafluorobiphenyl → 4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenyl

https://huagongshe.com/reaction/2304994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDecafluorobiphenylHCID 67949—
ReactantPotassiumHCID 5462222—
ReactantHCID 23672351HCID 23672351—
SolventDimethylformamideHCID 6228—
Product4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenylHCID 1087524492%

Reaction Conditions

Temperature-10 °C

Reaction Steps

37.4 g of decafluorobiphenyl (0.112 mol) are dissolved in 700 ml of dimethylformamide, the mixture is cooled to −10° C. using a cryostat, and a solution of 29.8 g of potassium 4-benzyloxycarbonylphenoxide (0.112mol) in 300 ml of dimethylformamide is then added dropwise over the course of 2 hours. After 48 hours at −10° C., the potassium salt has reacted. The dimethylformamide is then removed in a rotary evaporator, the residue is taken up in a little tetrahydrofuran, and the solution is filtered through a silica-gel column. The clear solution obtained is evaporated in a rotary evaporator until a white solid precipitates out. The solid is then stirred in n-hexane, filtered off using a fluted filter and then dried for 48 hours under nitrogen at 40° C./10 mbar in a vacuum drying cabinet (yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437178B2
Source datasetuspto-grants-2002_08
ORD IDord-4924021e330c435789a2980c8d0bf1fc
Source noteuspto-grants-2002_08