HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609837Generated: November 1, 2026
Tributyltin Chloride → 1-ethoxymethyl-2-tributylstannanyl-1H-imidazole
https://huagongshe.com/reaction/1609837
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 1-(Ethoxymethyl)-1H-imidazole | HCID 13019449 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-ethoxymethyl-2-tributylstannanyl-1H-imidazole | HCID 22260393 | — |
Reaction Steps
1.6 M n-BuLi (12.0 mL, 19.2 mmol) is slowly added to a solution of 1-ethoxymethyl-1H-imidazole (2.20 g, 17.4 mmol; prepared essentially as described by Tang, et al. (1978) J. Am. Chem. Soc. 100:3918) in THF (30 mL) at −78° C. under N2. The reaction mixture is stirred at −78° C. for 20 minutes, whereupon tributyltin chloride (5.7 mL, 20.9 mmol) is slowly added. The reaction mixture is stirred at −78° C. for 10 minutes, and then warmed to room temperature. After stirring at room temperature for 1.5 hours, the reaction mixture is concentrated in vacuo. The residue is triturated with hexanes and filtered, and the filtrate is concentrated in vacuo. The residue is again triturated with hexanes and filtered, and the filtrate concentrated in vacuo. The 1H NMR of the resulting oil indicates a 2:1 mixture of 1-ethoxymethyl-2-tributylstannanyl-1H-imidazole: 1-ethoxymethyl-1H-imidazole. This material is used in the next reaction without further purification. Selected 1H NMR resonances (400 MHz, CDCl3) δ 7.21 (s, 1H), 7.14 (s, 1H), 5.24 (s, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06982268B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-1f0b7b19356f4272b6f463def761abd9 |
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| Source note | uspto-grants-2006_01 |
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