HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 58309376, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Dithieno(3,2-b:2',3'-d)thiophene | HCID 137985 | — |
| Product | HCID 58309376 | HCID 58309376 | — |
Reaction Steps
Compound 2 was synthesized as shown in Scheme 2. Under acid condition, dithieno[3,2-b:2′,3′-d]thiophene (Organic Syntheses, Vol. 83, p. 209 (2006)) was reacted with NBS affording 2-bromodithieno[3,2-b:2′,3′-d]thiophene 7, which underwent Suzuki cross-coupling reaction with boronic acid R1—B(OH)2 (J. Mater. Chem., 2010, 20, 2182-2189) to afford intermediate 8 in 71% yields. Finally 8 was converted to PhN—OFFT-TCN by reacting with n-BuLi and tetracyanoethylene at low temperature in 85% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975419B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-2007015ef45546cfa189195043e83460 |
| Source note | uspto-grants-2015_03 |