HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzoylbenzoic acid → Tri-n-butyl-(4-benzoyl-benzoyloxy)-tin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzoylbenzoic acid | HCID 69147 | — |
| Reactant | Tributyltin methoxide | HCID 16683411 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Tri-n-butyl-(4-benzoyl-benzoyloxy)-tin | HCID 68508746 | 41.9% |
Reaction Steps
In a 50 ml dry three-neck-flask, 2.0 g (8.8 mmol) 4-benzoylbenzoic acid in 30 ml 1,2-dichlorethane are suspended under argon flow and heated to reflux. 2.8 g (8.8 mmol) tri-n-butylmethoxy tin are added slowly in the course of 0.5 h. The conversion is complete according to the 1H-NMR-spectrum. The slightly turbid hot solution is filtered, cooled and concentrated. 3.6 g of the crude product are obtained as yellowish oil. 2.4 g thereof are heated in a bulb-to-bulb distillation apparatus (0.03 mbar) and distilled at 190° C. 1.9 g of the title product is obtained as colorless oil. The structure is confirmed by 1H-NMR and 13C-NMR-spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318830B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-e127b5a293164734a91d62ff9df2e165 |
| Source note | uspto-grants-2012_11 |