Veratraldehyde → Methyl 1-(3,4-dimethoxybenzylamino)cyclopropanecarboxylate
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH:6]=O.Cl.[NH2:14][C:15]1([C:18]([O:20][CH3:21])=[O:19])[CH2:17][CH2:16]1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH2:6][NH:14][C:15]1([C:18]([O:20][CH3:21])=[O:19])[CH2:17][CH2:16]1Participants
3
Procedure
Prepared as in Example 12-1b from 3,4-dimethoxybenzaldehyde and methyl 1-aminocyclopropanecarboxylate hydrochloride. Yield 82%. MS 266 (MH+).
Sources & evidence
- ORD record
- ord-3798e6fd04eb41eea3fefe45dd74a14d
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08445692B2
Reaction notes
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