HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (6-Chloro-2-methylpyridin-3-YL)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Chloro-2-methylnicotinonitrile | HCID 12387737 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Chloro-2-methylpyridin-3-YL)methanamine | HCID 59534442 | — |
Reaction Steps
To a solution of 6-Chloro-2-methyl-nicotinonitrile (6 g) in THF (120 ml) at 25° C. was added NaBH4 (3 g) followed by the dropwise addition of BF3 etherate (6 ml). The reaction mixture was stirred for 3 h. MeOH (100 ml) and 2N HCl (100 ml) was added and refluxed for 1 h. The organic solvent was removed in vacuum and conc. NaOH (40 ml) was added followed by extraction with diethyl ether. The organic layer was separated, dried and concentrated in vacuum followed by filtration over silica gel (EtOAc/MeOH 80:20). The title compound was crystallized from MeOH/HCl (5.5 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE045323E1 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-f8fd971dead7488bb82dad890aff32aa |
| Source note | uspto-grants-2015_01 |