1-Chloro-2-(diethylamine)ethane hydrochloride → Ethanamine, N,N-diethyl-2-(2-(2-methylpropoxy)phenoxy)-
Reaction equation
[Na].[CH2:2]([O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[OH:13])[CH:3]([CH3:5])[CH3:4].Cl.[CH2:15]([N:17]([CH2:20][CH2:21]Cl)[CH2:18][CH3:19])[CH3:16]>C(O)C>[CH2:2]([O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:13][CH2:16][CH2:15][N:17]([CH2:20][CH3:21])[CH2:18][CH3:19])[CH:3]([CH3:5])[CH3:4]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound was prepared as described in Example 1, using sodium (2.3 g; 100 mole), o-isobutoxyphenol (8.30 g; 50 mmole) and diethylaminoethylchloride hydrochloride (8.6 g; 50 mmole) in 150 ml of ethanol. Yield 9.3 g (70%) of product, boiling at 112° C under a pressure of 0.01 mm Hg, nD25 : 1.4942.
Workup
- customThe compound was prepared
Sources & evidence
- ORD record
- ord-b951a5f7c3754c21877343fa0b8cdfbc
- Source dataset
- uspto-grants-1978_02
- Patent number
- US04073917
Reaction notes
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