N-Cyclohexylaniline → 2-(Cyclohexylphenylamino)ethanol
Reaction equation
C([O:3][C:4]([CH2:6][N:7]([CH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=O)C.C1(NC2C=CC=CC=2)CCCCC1>>[CH:14]1([N:7]([CH2:6][CH2:4][OH:3])[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1Participants
3
Procedure
N-ethoxycarbonylmethyl-N-cyclohexyl aniline 1.89 g was obtained from N-cyclohexyl aniline 1.30 g in the same manner as in the above example. This product 860 mg was reduced to give the title compound (300 mg, 42%).
Sources & evidence
- ORD record
- ord-12fbbaa6e32241d587f92ac37f2a3e9d
- Source dataset
- uspto-grants-2004_05
- Patent number
- US06737425B1
Reaction notes
Loading…