Benzenamine, 3,5-bis(trifluoromethyl)- → HCID 15484846, compound
Reaction equation
FC(F)(F)C1C=C(C=C(C(F)(F)F)C=1)N.C([O:20][C:21](=[O:39])[C@H:22]([CH3:38])[NH:23][C:24]1[CH:29]=[C:28]([C:30]([F:33])([F:32])[F:31])[CH:27]=[C:26]([C:34]([F:37])([F:36])[F:35])[CH:25]=1)C(C)C>>[F:31][C:30]([F:32])([F:33])[C:28]1[CH:29]=[C:24]([NH:23][C@H:22]([C:21]([OH:39])=[O:20])[CH3:38])[CH:25]=[C:26]([C:34]([F:37])([F:36])[F:35])[CH:27]=1Participants
3
Procedure
Following General Procedure J and using 3,5-di(trifluoromethyl)aniline (Aldrich) and isobutyl R-(+)-lactate (Aldrich), N-[3,5-di(trifluoromethyl)phenyl]-L-alanine isobutyl ester was prepared as an oil. The reaction was monitored by silica gel tic (Rf=0.38 in 10% EtOAc/hexanes). Purification was by preparative plate thin layer chromatography using 10% EtOAc/hexanes as the eluant.
Workup
- customwas prepared as an oil
- customPurification
Sources & evidence
- ORD record
- ord-39c12f2fadd24924b9630764a48f6c89
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06495693B2
Reaction notes
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