Diethylethanolamine → HCID 53920903, compound
Reaction equation
[CH2:1]([N:3]([CH2:7][CH3:8])[CH2:4][CH2:5][OH:6])[CH3:2].[O:9]=[C:10]1[C:16]2[CH:17]=[CH:18][C:19]([C:21](OCCN(C)C)=[O:22])=[CH:20][C:15]=2[CH:14]=[CH:13][C:12]2[CH:29]=[CH:30][CH:31]=[CH:32][C:11]1=2>>[O:9]=[C:10]1[C:16]2[CH:17]=[CH:18][C:19]([C:21]([O:6][CH2:5][CH2:4][N:3]([CH2:7][CH3:8])[CH2:1][CH3:2])=[O:22])=[CH:20][C:15]=2[CH:14]=[CH:13][C:12]2[CH:29]=[CH:30][CH:31]=[CH:32][C:11]1=2Participants
3
Procedure
In similar manner substituting diethylethanolamine for the dimethylethanolamine, there is obtained β-N,N-diethylaminoethyl (5-oxo-5H-dibenzo[a,d]cyclohepten-2-yl)carboxylate.
Sources & evidence
- ORD record
- ord-bf079e96c1614884b240c87d4aa22d8f
- Source dataset
- uspto-grants-1977_07
- Patent number
- US04035509
Reaction notes
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