HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → 3,N,N-trimethyl-4-(2-triphenylsilanylsulfanyl-ethyl)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Triphenylsilanethiol | HCID 621128 | — |
| Reactant | 3,N,N-Trimethyl-4-vinylbenzamide | HCID 66816211 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,N,N-trimethyl-4-(2-triphenylsilanylsulfanyl-ethyl)-benzamide | HCID 86672758 | 69% |
Reaction Steps
A mixture of 3,N,N-trimethyl-4-vinyl-benzamide (706 mg, 3.73 mmol), triphenylsilanethiol (1.76 g, 6.00 mmol) and AIBN (185 mg, 1.13 mmol) in toluene (16 ml) was heated with stirring at 88° C. for two hours in a sealed test tube in an N2 atmosphere. The reaction mixture was cooled to room temperature and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1) to give 3,N,N-trimethyl-4-(2-triphenylsilanylsulfanyl-ethyl)-benzamide (1.24 g, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169254B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-886234ea72eb430e950773cdd21d10f0 |
| Source note | uspto-grants-2015_10 |