2-Aminomethyl-4,4,8-trimethyl-nonanoic acid → 2-Aminomethyl-4-ethyl-8-methyl-nonanoic Acid
Reaction equation
[NH2:1][CH2:2][CH:3]([CH2:7][C:8]([CH3:16])(C)[CH2:9][CH2:10][CH2:11][CH:12]([CH3:14])[CH3:13])[C:4]([OH:6])=[O:5].N[CH2:18]C(CCCCCC(C)C)C(O)=O.C1(C(OC2C(C(C)(C)C)=CC(C)=CC=2C(C)(C)C)=O)CC1>>[NH2:1][CH2:2][CH:3]([CH2:7][CH:8]([CH2:16][CH3:18])[CH2:9][CH2:10][CH2:11][CH:12]([CH3:13])[CH3:14])[C:4]([OH:6])=[O:5]Participants
4
Procedure
A procedure similar to that of 2-Aminomethyl-4,4,8-trimethyl-nonanoic acid was utilized to prepare 2-Aminomethyl-8-methyl-nonanoic acid from 2,6-di-t-butyl-4-methylphenyl cyclopropylcarboxylate. m/z 230.2 (M+).
Sources & evidence
- ORD record
- ord-4d674bab85114f5d8a04bcbc4e162452
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07419981B2
Reaction notes
Loading…