HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 5-(3,4-Dihydro-1-isoquinolinyl)-3-nitropyrocatechol hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1-(3,4-Dimethoxy-5-nitrophenyl)-3,4-dihydroisoquinoline | HCID 21458983 | — |
| Product | 5-(3,4-Dihydro-1-isoquinolinyl)-3-nitropyrocatechol hydrobromide | HCID 135665329 | — |
Reaction Steps
1.4 g of 1-(3,4-dimethoxy-5-nitrophenyl)-3,4-dihydroisoquinoline are treated with 15 ml of constant-boiling hydrobromic acid and heated to boiling under reflux under a nitrogen atmosphere for 1.5 hours. After distilling the hydrobromic acid in a water-jet vacuum, the crystalline residue is recrystallized from acetone. There is obtained 5-(3,4-dihydro-1-isoquinolinyl)-3-nitropyrocatechol hydrobromide in the form of yellow crystals of m.p. >250° (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705703 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-1bba47e3c1a447eeb0d356fd6dc35985 |
| Source note | uspto-grants-1998_01 |