HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382912Generated: October 25, 2026
4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenyl → HCID 11814689, compound
https://huagongshe.com/reaction/382912
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(4-Benzyloxycarbonylphenoxy)nonafluorobiphenyl | HCID 10875244 | — |
| Reactant | HCID 11781031 | HCID 11781031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11814689 | HCID 11814689 | 94% |
Reaction Steps
49.9 g of the 4-(4-benzyloxycarbonylphenoxy)nonafluorobiphenyl (0.092 mol) prepared as described in Example 1 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 Büchner funnel and subsequently dried for 48 hours under nitrogen,at 40° C./10 mbar in a vacuum drying cabinet (yield: 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310238B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-311d9468de894b9abc953a4376753053 |
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| Source note | uspto-grants-2001_10 |
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