HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichlorobenzene → 1-(2-Bromophenyl)isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | 1-(2-Bromophenyl)-3,4-dihydroisoquinoline | HCID 10779537 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2-Bromophenyl)isoquinoline | HCID 11403358 | — |
Reaction Conditions
| Temperature | 180 °C |
|---|
Reaction Steps
A mixture of 28.6 g (100 mmol) of 1-(2-bromophenyl)-3,4-dihydroisoquinoline, 86.9 g (1 mol) of manganese dioxide and 200 ml of 1,2-dichlorobenzene was stirred at 180° C. for 5 h. After cooling, the mixture was diluted with 500 ml of toluene and filtered through silica gel. After the solvent had been removed, the product was obtained as a yellow oil. The yield at a purity of approx. 99.0% was 26.0 g (91 mmol), 91.4% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820822B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-9938ca1c516e454e9e3d85c01e6cd1a8 |
| Source note | uspto-grants-2010_10 |