HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl bromide → 1-Methylbut-1-en-3-onyltin bromide dichloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl bromide | HCID 12056 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Methylbut-1-en-3-onyltin bromide dichloride | HCID 85766639 | 65% |
Reaction Steps
39.8 g (0.21 mol) of tin(II) chloride and 21.0 g (0.21 mol) of acetylacetone in 200 ml of diethyl ether were placed in a reactor. 38.8 g (0.21 mol) of benzoyl bromide were metered in over 15 min at room temperature, with stirring, a rise in temperature to the reflux point being recorded. After a postreaction time of 1 h at the reflux temperature, the mixture was cooled and the crystalline precipitate was separated off. 48 g (65% of theory) of 1-methylbut-1-en-3-onyltin bromide dichloride (BrCl2Sn--C(CH3)=CH--CO--CH3) were isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05817851 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-74cd980bc0894e0cb08fba6a83e17bf6 |
| Source note | uspto-grants-1998_10 |