HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 6-Fluoro-1,2,3,4-tetrahydronaphthalen-1-one | HCID 14915116 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-amine | HCID 16244337 | — |
Reaction Steps
Over a solution of 6-fluorotetralone (6-fluoro-3,4-dihydro-1 H-naphthalen-2-one; 1 equivalent) and ammonium acetate (5 equivalents) in a 2:1 mixture of MeOH:THF (0.24 M), was carefully added NaCNBH3 (2 eq), and the reaction mixture was stirred at room temperature for 2 hours. Concentrated HCl was added at 0° C. until the pH was less than 2, and the MeOH was removed in vacuo. The residue was taken up in water and extracted with CHCl3 (2×). The aqueous solution was basified with solid KOH and extracted with CHCl3 (3×). The combined extracts were dried (MgSO4) and evaporated in vacuo to give the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06638927B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-396b1468175f47059e069502df5eca4d |
| Source note | uspto-grants-2003_10 |