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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304995Generated: October 25, 2026

4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenyl → HCID 11814689, compound

https://huagongshe.com/reaction/2304995

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenylHCID 10875244—
ReactantHCID 11781031HCID 11781031—
SolventDimethylformamideHCID 6228—
ProductHCID 11814689HCID 1181468994%

Reaction Conditions

Temperature80 °C

Reaction Steps

49.9 g of the 4-(4-benzyloxycarbonylphenoxy)nonafluorobiphenyl prepared as described in Example 1 (0.092 mol) and 26.1 g of potassium 4-nitro-3-benzyloxyphenoxide (0.092 mol) are dissolved in 400 ml of dimethylformamide, and the solution is heated to 80° C.; the reaction is complete after 24 hours. The solvent is then removed in a rotary evaporator. The solid residue obtained is washed three times with methanol, filtered off via a Buchner funnel and subsequently dried for 48 hours under nitrogen at 40° C./10 mbar in a vacuum drying cabinet (yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437178B2
Source datasetuspto-grants-2002_08
ORD IDord-0ed4674c54764ac1a9c022cafac80c2b
Source noteuspto-grants-2002_08