4-(Trifluoromethoxy)benzylamine → HCID 58230102, compound
Reaction equation
C(O[C:4]([C:6]1([CH2:13][CH2:14]OC)[CH2:11][CH2:10][CH:9]([OH:12])[CH2:8][CH2:7]1)=[O:5])C.[F:17][C:18]([F:29])([F:28])[O:19][C:20]1[CH:27]=[CH:26][C:23]([CH2:24][NH2:25])=[CH:22][CH:21]=1>>[OH:12][CH:9]1[CH2:8][CH2:7][C:6]2([C:4](=[O:5])[N:25]([CH2:24][C:23]3[CH:26]=[CH:27][C:20]([O:19][C:18]([F:17])([F:28])[F:29])=[CH:21][CH:22]=3)[CH2:14][CH2:13]2)[CH2:11][CH2:10]1Participants
3
Procedure
The title compound was prepared in analogy to example 108, step 3 from 4-hydroxy-1-(2-methoxy-ethyl)-cyclohexanecarboxylic acid ethyl ester (obtained in example 2, step 3) by treatment with 4-trifluoromethoxybenzylamine as a mixture of cis and trans diastereomers. Light yellow viscous oil. MS (m/e): 344.147 [MH+].
Sources & evidence
- ORD record
- ord-6058f0405fff42879dba8ddca9031610
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08440710B2
Reaction notes
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