Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Decanoyl chloride | HCID 66982 | — |
| Reactant | Dimethylformamide toluene | HCID 21735183 | — |
| Reactant | HCID 178516123 | HCID 178516123 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178443445 | HCID 178443445 | — |
Reaction Steps
6.1 g (0.014 mol) of bis(cyclopentadienyl)bis(2,6-difluoro-3-hydroxyphenyl)titanium and 2.7 g (0.0336 mol) of pyridine in 50 ml of a toluene/DMF mixture (1:1) are introduced into a 100 ml sulfation flask under nitrogen as protective gas. 6.4 g (0.0336 mol) of decanoyl chloride are added dropwise to this red solution at room temperature over the course of 5 minutes, and the mixture is stirred for a further 16 hours (reaction check using thin-layer chromatography). The reaction mixture is then poured into ether and water. The ether phase is evaporated off, washed twice with water, dried using magnesium sulfate and evaporated on a rotary evaporator. The residue is purified by flash chromatography using a hexane/ether mixture 9:1 as eluent, and evaporated on a rotary evaporator. 6.9 g of a red, clear resin are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05192642 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-96c2fa6b88ac419aa391d6f44589aaec |
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| Source note | uspto-grants-1993_03 |
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