Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 2,5-Dibromothiophene | HCID 18453 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 69978577 | HCID 69978577 | — |
Reaktionsschritte
To 2,5-Dibromothiophene (1.5 g, 6.2 mmol in THF (30 mL) cooled to −78° C. was added lithium diisopropylamide (6.2 mL, 6.2 mmol; 1.0M in THF, 6.2 mmol;) dropwise. The mixture was stirred 5 min, and was quenched with DMF (1.4 g, 18.6 mmol). Stirring was continued for 15 min at −78° C. and water was added. The THF was evaporated, Et2O was added and the organic phase was separated and washed with water, 1% HCl, water (3×) and brine. The organic phase was passed through a silica plug and toluene (20 mL) was added. Methyl(triphenylphosphonanylidene) acetate (3.34 g, 10.0 mmol) was added at 23° C. and the mixture was stirred for 12 h. The solvents were then evaporated, ether was added and the mixture was passed through a silica plug. The mixture was concentrated in vacuo and dried overnight via high vacuum and 585 mg of the above named enoate was obtained as a tan solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06359181B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-b2e5337e512d4d0591f23cacaa251d7a |
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| Quellennotiz | uspto-grants-2002_03 |
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