HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 6-Hydroxy-2-n-octyl-1,2,3,4-tetrahydroisoquinoline hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 6-Methoxy-2-n-octyl-1,2,3,4-tetrahydroisoquinoline | HCID 20155816 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Hydroxy-2-n-octyl-1,2,3,4-tetrahydroisoquinoline hydrobromide | HCID 20155810 | — |
Reaction Steps
5.8 g of the compound prepared under (b) are heated under reflux for 16 hours with a mixture of 100 ml of glacial acetic acid and 48% strength aqueous hydrobromic acid in the volume ratio 1:1. After cooling, the acid mixture is distilled off under waterpump vacuum, and the residue is boiled with a little ethanol. On cooling and scratching, 4.0 g of colorless crystals crystallize out (47% of theory over all stages), melting point: 165-166°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04717724 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-c8489944588f49dd8d67431ae73ccebf |
| Source note | uspto-grants-1988_01 |