4-Ethoxyaniline → HCID 67131106, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:10]=[CH:9][C:7]([NH2:8])=[CH:6][CH:5]=1)[CH3:2].[C:11]([Si:15]([CH3:23])([CH3:22])[O:16][CH2:17][CH2:18][C@@H:19]1[CH2:21][O:20]1)([CH3:14])([CH3:13])[CH3:12]>CC(=O)OCC>[C:11]([Si:15]([CH3:23])([CH3:22])[O:16][CH2:17][CH2:18][C@@H:19]([OH:20])[CH2:21][NH:8][C:7]1[CH:9]=[CH:10][C:4]([O:3][CH2:1][CH3:2])=[CH:5][CH:6]=1)([CH3:12])([CH3:14])[CH3:13]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Starting from 4-ethoxyaniline (3.2 mL; commercial) and tert-butyl-dimethyl-((R)-2-oxiranyl-ethoxy)-silane (5.0 g; prepared according to WO 2007/144423) and following procedure A, the title compound was obtained after CC (EA/Hept 1:1) as a brown oil (5.22 g; 62% yield).
Sources & evidence
- ORD record
- ord-c4097e82a4de4c02a7ebae63cb74f92f
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08349826B2
Reaction notes
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