HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898642Generated: October 30, 2026
Tributyltin Chloride → 4-tributylstannanyl-1-(2,3,5-trifluoro-phenyl)-1H-imidazole
https://huagongshe.com/reaction/1898642
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-iodo-1-(2,3,5-trifluorophenyl)-1H-imidazole | HCID 57516655 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-tributylstannanyl-1-(2,3,5-trifluoro-phenyl)-1H-imidazole | HCID 57516656 | — |
Reaction Steps
A solution of 4-iodo-1-(2,3,5-trifluorophenyl)-1H-imidazole (0.140 g, 0.43 mmol) in 2 mL of THF under Ar was chilled in an ice/water bath 5 min. Isopropylmagnesium chloride (2.0 M in tetrahydrofuran, 0.225 mL, 0.45 mmol) was added, the bath was removed, and the pale yellow solution was stirred for 1.5 h. Tributyltin chloride (0.055 mL, 0.20 mmol) was added all at once, and the pale yellow solution was stirred 1 h. A sat. aq. NH4Cl solution (10 mL) was added, and the mixture was extracted with two 10 mL portions of EtOAc. The combined organic layers were washed with 10 mL of a sat. aq. NaCl solution, dried over Na2SO4, filtered and concentrated to give 4-tributylstannanyl-1-(2,3,5-trifluoro-phenyl)-1H-imidazole as a yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08518945B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-4d86e693c3334ad7bcc2806afed3319a |
|---|
| Source note | uspto-grants-2013_08 |
|---|