Hydrochloric Acid → HCID 21288106, compound
Reaction equation
[CH3:1][N:2]([CH3:10])[CH2:3][CH:4]([OH:9])[CH2:5][N:6]([CH3:8])[CH3:7].[ClH:11]>>[ClH:11].[ClH:11].[CH3:1][N:2]([CH3:10])[CH2:3][CH:4]([OH:9])[CH2:5][N:6]([CH3:8])[CH3:7]Participants
Procedure
A 1000 mL four-neck flask equipped with a reflux condenser, mechanical stirrer, thermometer and a dropping funnel was charged with 149.5 g (1.0 mole) of a 98 percent, N,N,N',N'-tetramethyl-2-hydroxy-1,3-propanediamine. The flask was immersed into an ice-water bath while 197.2 g (2.0 moles) of concentrated hydrochloric acid was introduced at such a rate as to keep the temperature between 35° and 45° C. To the N,N,N',N'-tetramethyl-2-hydroxy-1,3-propanediamine dihydrochloride so obtained, 185.0 g (2.0 moles) of epichlorohydrin was added slowly, taking care that the temperature did not exceed 45° C. After the addition was completed, the temperature was raised to between 60° and 71° C. for 30 minutes. A 77.2 percent solution of the title compound was obtained.
Workup
- customA 1000 mL four-neck flask equipped with a reflux condenser, mechanical stirrer
- additionwas introduced at such a rate as
- customthe temperature between 35° and 45° C
Sources & evidence
- ORD record
- ord-415d5e24d68943a5a60d08a22a22ed44
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04778813
Reaction notes
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