Hydrogen Bromide → HCID 21332375, compound
Reaction equation
Br.[CH2:2]([N:19]([CH2:21][CH:22]([OH:29])[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])C)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][N:8]([CH2:10][CH:11]([OH:18])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])C>>[CH2:2]([NH:19][CH2:21][CH:22]([OH:29])[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][NH:8][CH2:10][CH:11]([OH:18])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]Participants
3
Procedure
In a manner similar to that of Example 22, methylation of N,N'-(1,6-hexylene)-bis[2-hydroxyoctylamine] (35 g.) and treatment of the resulting product (b.p. 177°-182° C./l mm.) with hydrogen bromide gave N,N'-(1,6-hexylene)-bis[N-methyl-2-hydroxyoctylamine] (I: R = CH3 (CH2)5, R' = CH3, X = (CH2)6, Z = H) dihydrobromide (19.1 g., m.p. 167.0°-168.8° C.).
Sources & evidence
- ORD record
- ord-82053c4511084a4fa511706edfd134b6
- Source dataset
- uspto-grants-1978_04
- Patent number
- US04085144
Reaction notes
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