HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Methyl-7-nitro-3,4-dihydroisoquinoline | HCID 10932228 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline | HCID 21584311 | 82.5% |
Reaction Steps
1.08 g of 1-methyl-7-nitro-3,4-dihydroisoquinoline was dissolved in 10 ml of methanol, and 0.43 g of sodium borohydride was added to the solution at 0° C. The solution was stirred overnight at room temperature, and water was added to the reaction mixture. The mixture was extracted with ethyl acetate, and after washing with saturated aqueous solution of sodium chloride, the solution was dried with anhydrous sodium sulfate. The desiccant was separated by filtration, and the filtrate was purified by silica gel column chromatography to obtain 0.90 g of 1-methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline, which was an oily product (yield: 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05789595 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-a27e714908bf4ba4b1cf51f6fb4b7765 |
| Source note | uspto-grants-1998_08 |