HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-(6-Phenylhex-1-yn-1-yl)quinoline-8-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Phenyl-1-hexyne | HCID 136908 | — |
| Reactant | 5-Bromoquinoline-8-carboxaldehyde | HCID 16414243 | — |
| Catalyst | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(6-Phenylhex-1-yn-1-yl)quinoline-8-carbaldehyde | HCID 86672376 | 56.7% |
Reaction Steps
A solution of 5-bromo-8-quinolinecarboxaldehyde (987 mL, 418 mmol), 5-hexyn-1-yl-benzene [CAS 100848-88-2] (1.05 mL, 5.85 mmol), triethylamine (2 mL) and 1,3-bis(diphenylphosphino)propane (dppp, 59 mg) in DMF (10 mL) was heated to 90° C. with stirring for 2 h. After cooling to RT, the reaction mixture was extracted with ether and washed with water and brine, dried over magnesium sulfate and concentrated. Purification by MPLC (35% ethyl acetate in hexanes) gave rise to 1.04 g of Intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658634B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-1f47f1346da04abebcd68aef14693174 |
| Source note | uspto-grants-2014_02 |