Phenethyl bromide → N-(2-Phenylethyl)aminoacetaldehyde diethyl acetal
Reaction equation
[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[CH2:5][NH2:6])[CH3:2].Br[CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[CH2:5][NH:6][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH3:2]Participants
3
Procedure
According to the procedure described in the synthesis method of Compound IX-1, 2,2-diethoxyethanamine (5.82 ml, 40 mmol) was reacted with (2-bromoethyl)benzene (2.70 ml, 20 mmol) and the obtained residue was purified by Büch silica gel column chromatography (chloroform only) to obtain the title compound (4.45 g, 94%).
Workup
- customthe obtained residue was purified by Büch silica gel column chromatography (chloroform only)
Sources & evidence
- ORD record
- ord-4a6e66be2fbc4b9782da961247b0030a
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09126981B2
Reaction notes
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