HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → 5-Bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 5-Bromo-8-nitroisoquinoline | HCID 816983 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinoline | HCID 10016010 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
5-Bromo-8-nitroisoquinoline (216.9 g, 0.86 mol) was added in portions during 10 min to a solution of dimethylsulphate (750 ml). Some heat was developed. The mixture was heated at 100° C. for 10 minutes. 5-Bromo-2-methyl-8-nitroquinolinium methyl sulphate precipitated. The mixture was cooled on ice and diethyl ether (1 l) was added. The crude mixture was filtered and crystals were isolated. The salt was solved in acetic acid (1.5 l). To the ice-cooled mixture was added: sodium borohydride (47 g, 1.24 mol) over 4 hours. The temperature was kept below 30° C. The crude mixture was evaporated and sodium hydroxide (2 l, 1 M) was added. The crystals were filtered. Yield 205.2 g (88%). Mp 85-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07282511B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-6a679fbecc35413abec6e948c4bcf4a6 |
| Source note | uspto-grants-2007_10 |