Ethylamine → 3,5-Dichloro-N-ethyl-2-hydroxybenzamide
Reaction equation
[Cl:1][C:2]1[C:3]([OH:12])=[C:4]([CH:8]=[C:9]([Cl:11])[CH:10]=1)[C:5]([OH:7])=O.[CH2:13]([NH2:15])[CH3:14]>>[Cl:1][C:2]1[C:3]([OH:12])=[C:4]([CH:8]=[C:9]([Cl:11])[CH:10]=1)[C:5]([NH:15][CH2:13][CH3:14])=[O:7]Participants
3
Procedure
The title compound was prepared from 3,5-dichloro-2-hydroxybenzoic acid and ethylamine, using a similar method to that of preparation 52, to afford the title compound as a pale yellow solid. 1HNMR (400 MHz, CDCl3) δ: 1.28 (3H, t), 3.47-3.54 (2H, m), 6.29-6.36 (1H, bs), 7.27 (1H, d), 7.48 (1H, d); LRMS ESI m/z 232 [M−H]−
Workup
- customof preparation 52
Sources & evidence
- ORD record
- ord-1de847e7e3a64212b066711a4261700c
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07547731B2
Reaction notes
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