Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 20561020 | HCID 20561020 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 12766301 | HCID 12766301 | 56% |
Reaction Steps
2,3-bis(4-Methoxyphenyl)-5-(2,4-dinitrophenylthio)thiophene (4.9 g, 10 mmoles), tetrahydrofuran (60 ml), methanol/water (7.5 ml, 2.5 ml) and potassium hydroxide (1.3 g, 20 mmoles) were charged into a stainless steel bomb. The bomb was briefly evacuated, charged with tetrafluoroethylene (5 g, 50 mmoles) and agitated for 12 hours at room temperature. The reaction mixture was filtered and the filtrate concentrated to near dryness. The residue was taken up in ethyl acetate and filtered. The filtrate was washed three times with 1 N NaOH, three times with 1 N HCl, once with brine, dried and concentrated in vacuo. Crystallization from ethanol/water gave the title compound (2.4 g), m.p. 84°-7° (D). Infrared and H-NMR spectra were consistent with the assigned structure. MS 428 (M+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04302461 |
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| Source dataset | uspto-grants-1981_11 |
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| ORD ID | ord-d275c25a1fd54e38828871feeea60ce7 |
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| Source note | uspto-grants-1981_11 |
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