Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Titanium Tetrachloride | HCID 24193 | — |
| Reactant | Trimethylsilyl-cyclopentadienyl-dichloroborane | HCID 131722197 | — |
| Product | HCID 178477808 | HCID 178477808 | — |
Reaction Steps
11.4 g (0.052 mole) of compound 2 and 100 ml methylene chloride (CH2Cl2) were placed in a 250 ml Schlenk tube. These solution was cooled to −78° C. and 9.8 g (5.6 ml, 0.052 mole) titanium tetrachloride were added drop-wise over 10 minutes. The red solution obtained was slowly heated to room temperature and was stirred for a further 3 hours. The solvent was removed under vacuum, whereupon a yellowish product was obtained. 200 ml hexane were added to the crude solid, and yellow solution obtained was filtered and cooled overnight in a refrigerator, whereupon 12.3 g (79% of the theoretical yield) of yellow crystals of compound 3 were obtained. It should be mentioned that in J. Organometallic Chem. 169 (1979), 373, 62% of the theoretical yield was obtained when the reaction was conducted in a hydrocarbon solvent such as petroleum ether or methylcyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06423659B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-8970df1f5d1447789e287f714cb8232b |
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| Source note | uspto-grants-2002_07 |
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