HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 67138806, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Methyl-thiophene-2-carboxylic acid 2-trimethylsilanylethyl ester | HCID 67138429 | — |
| Catalyst | Mercury | HCID 23931 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 67138806 | HCID 67138806 | — |
Reaction Steps
A solution of the title A compound, 5-methyl-thiophene-2-carboxylic acid 2-trimethylsilanyl-ethyl ester (34.15 g, 141 mmol) in CCl4 (200 mL) is treated with N-bromosuccinimide (NBS, 25.08 g, 141 mmol) and 2,2′-azobisisobutyronitrile (1.0 g, 6 mmol). The mixture is irradiated with a 450 W mercury lamp for 3 h. An additional 2.5 g of NBS is added and the mixture is further irradiated for 2 h. The mixture is filtered through Celite and a plug of silica gel. The solvent is evaporated to give 5-bromomethyl-thiophene-2-carboxylic acid 2-trimethylsilanyl-ethyl ester as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291635B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-5a721372e7a4485aab64850f49bc6764 |
| Source note | uspto-grants-2007_11 |