HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyltin chloride → Trimethyl (5-methyl-2-benzofuranyl)stannane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | 5-Methylbenzofuran | HCID 33103 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Trimethyl (5-methyl-2-benzofuranyl)stannane | HCID 85673465 | 102.4% |
Reaction Steps
n-Butyl lithium (1.57M in hexane, 75 ml) was added dropwise to a stirred solution of 5-methylbenzofuran (14 g) in dry THF (150 ml) at -70° under nitrogen over 45 min. The solution was then allowed to warm to -55° before a solution of trimethyltin chloride (23 g) in THF (70 ml) was added dropwise. The solution temperature rose to -32°. The cooling bath was removed and the solution was stirred at room temperature for 2 h. The solution was diluted with ethyl acetate (250 ml) and washed with water (200 ml). The organic layer was dried and concentrated in vacuo to afford a yellow liquid (32 g). Kugelrohr distillation of this liquid gave the title compound (23.3 g) as a colourless liquid, b.p. 115° at 7 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05317023 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-400980ffcf014dc18caf2aa99952806d |
| Source note | uspto-grants-1994_05 |