HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898635Generated: November 1, 2026
Tributyltin Chloride → HCID 57516653, compound
https://huagongshe.com/reaction/1898635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 57516652 | HCID 57516652 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57516653 | HCID 57516653 | 111.1% |
Reaction Steps
A solution of 1-(2,5-difluorophenyl)-4-iodo-1H-imidazole (0.115 g, 0.38 mmol) in 2 mL of tetrahydrofuran was chilled in an ice/water bath 5 min. Isopropylmagnesium chloride solution (2.0 M in tetrahydrofuran, 0.190 mL, 0.38 mmol) was added all at once. The bath was removed, and the pale yellow solution stirred 1.5 h. Tributyltin chloride (0.105 mL, 0.39 mmol) was added all at once, and the pale yellow solution was stirred 1.5 h. A sat. aq. NH4Cl solution (10 mL) was added, and the mixture was extracted with two 10 mL portions of ethyl acetate. The combined organic layers were washed with 20 mL of a sat. aq. NaCl solution, dried over Na2SO4, filtered and concentrated to provide 0.198 g of 1-(2,5-difluoro-phenyl)-4-tributylstannanyl-1H-imidazole as a yellow oil which was used without further purification. MS: (M+H)+=471.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08518945B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-15984c3ba9274043a76d51f70ebc6c08 |
|---|
| Source note | uspto-grants-2013_08 |
|---|