HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Tri-n-butylstannyl)thiophene → HCID 67042477, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| Reactant | HCID 67042476 | HCID 67042476 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67042477 | HCID 67042477 | — |
Reaction Steps
To the mixture of bis(2-butyl-1-octyl) 5,5′-dibromo-2,2′-bithiophene-4,4′-dicarboxylate (1.00 g, 1.34 mmol) and 2-tributylstannylthiophene (1.50 g, 4 mmol) was added Pd(PPh3)4 (46 mg, 0.04 mmol), and anhydrous DMF (15 ml). The mixture was placed under vacuum and flushed with argon several times and was put on a microwave reactor with a setting of 160° C. for 60 min. The reaction mixture was cooled to room temperature and the solvent was removed. The residue was washed with methanol to remove traces of DMF. After drying, the liquid was dissolved in hexane and purified twice by column chromatography on silica gel using a mixture of hexane/ethyl acetate (9/1) (Rf=0.5). A light yellow liquid was obtained. Yield: 1.01 g (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08624232B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-6bd8741ed46b48b491daf06457267eba |
| Source note | uspto-grants-2014_01 |