Acetonitrile → 1-[4-(Hydroxymethyl)piperidin-1-yl]ethan-1-one
Reaction equation
OC[C:3]([NH:6][C:7](=[O:9])[CH3:8])([CH3:5])C.N1CC[CH:13]([CH2:16][OH:17])[CH2:12][CH2:11]1.CC#N.O.CC#N>O>[OH:17][CH2:16][CH:13]1[CH2:5][CH2:3][N:6]([C:7](=[O:9])[CH3:8])[CH2:11][CH2:12]1Participants
6
Procedure
The title compound is prepared analogously as described for N-(2-hydroxy-1,1-dimethyl-ethyl)-acetamide from piperidin-4-yl-methanol. MS (LC-MS): [M+H]+=158.3. tR (HPLC, Waters Symmetry C18 column, 5-95% CH3CN/H2O/3.5 min, 95% CH3CN/H2O, 2 min, CH3CN and H2O containing 0.1% TFA, flow: 0.6 mL/min): 0.39 min.
Workup
- custom0.39 min.
Sources & evidence
- ORD record
- ord-772d7d903336432db83eab4c3c1c8fd0
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07807709B2
Reaction notes
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