tert-butyl N-(2-hydroxyethyl)carbamate → Methyl 2-(2-tert-butoxycarbonylaminoethoxy)-4-(methyl-thio)benzoate
Reaction equation
[OH:1][C:2]1[CH:11]=[C:10]([S:12][CH3:13])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[C:14]([O:18][C:19]([NH:21][CH2:22][CH2:23]O)=[O:20])([CH3:17])([CH3:16])[CH3:15]>>[C:14]([O:18][C:19]([NH:21][CH2:22][CH2:23][O:1][C:2]1[CH:11]=[C:10]([S:12][CH3:13])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5])=[O:20])([CH3:17])([CH3:16])[CH3:15]Participants
3
Procedure
Methyl 2-[2-(tert-butoxycarbonylamino)ethoxy]-4-(methylthio)benzoate was prepared (12.6 g, 76%) as described in Example 21-C from methyl 2-hyroxy-4-(methylthio)benzoate and 2-(tert-butoxycarbonylamino)ethanol.
Sources & evidence
- ORD record
- ord-566e657c41044de683adcbd3ff2b915b
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07700628B2
Reaction notes
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