HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719083Generated: October 31, 2026
Tributyltin fluoride → HCID 178504582, compound
https://huagongshe.com/reaction/719083
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin fluoride | HCID 16120 | — |
| Reactant | HCID 178504581 | HCID 178504581 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178504582 | HCID 178504582 | — |
Reaction Steps
To a murky green-yellow solution of rac-dimethylsilyl-bis (tetrahydroindenyl) zirconium dichloride [DMS bis (THI) ZrCl2] (1.00 g, 2.19 mmol, 1.00 eq.) in dichloromethane (15 mL) was added tributyltin fluoride (1.42 g, 4.59 mmol, 2.10 eq.). The reaction lightened immediately. The reaction was stirred for one hour and was then filtered to give a straw-yellow solution and a small amount of brownish solid. The solution was then evaporated in vacuo, leaving a manila-colored, thick suspension. The suspension was washed with pentane (20 mL, then 3×5 mL) to give a white, micro crystalline solid. The solid was dried in vacuo to yield 0.76 g (82%). 1H NMR (CD2Cl2): δ 0.80 (s, 6H, SiMe2, 1.45–1.9 and 2.4–2.7 (br m, 16H, aliphatic-ring-H), 5.61 (d, 2H, cyclopentadienyl-ring-H), 6.27 (br s, 2H, cyclopentadienyl-ring-H). 19F NMR (CD2Cl2): δ 19.9 (s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132382B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-948f7e175640492b98f7c9a38557aeb4 |
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| Source note | uspto-grants-2006_11 |
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