Hydrochloric Acid → Hydrochloric Acid
Reaction equation
[OH:1][CH2:2][C:3]1[CH2:4][N:5](C(OC(C)(C)C)=O)[CH2:6][CH2:7][C:8]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[ClH:22]>O1CCOCC1>[C:9]1([C:8]2[CH2:7][CH2:6][NH:5][CH2:4][C:3]=2[CH2:2][OH:1])[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1.[ClH:22]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
To tert-butyl 3-(hydroxymethyl)-4-phenyl-5,6-dihydropyridine-1(2H)-carboxylate (510 mg, 1.76 mmol) was added 4N HCl in Dioxane (3 ml), after stirring at room temperature for 1 h, it was concentrated to give (4-phenyl-1,2,5,6-tetrahydropyridin-3-yl)methanol as HCl salt.
Workup
- concentrationit was concentrated
Sources & evidence
- ORD record
- ord-ce51e956026d453f8075934d6d0f3f92
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09422279B2
Reaction notes
Loading…