Dimethylamine → HCID 11286707, compound
Reaction equation
[CH:1]1[C:6]([CH2:7]Cl)=[CH:5][CH:4]=[C:3]([Cl:9])[CH:2]=1.[CH3:10][NH:11][CH3:12]>O1CCCC1.C(OCC)C>[CH3:10][N:11]([CH2:7][C:6]1[CH:5]=[CH:4][C:3]([Cl:9])=[CH:2][CH:1]=1)[CH3:12]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The starting material is prepared as follows: The solution of 141 g of α,p-dichlorotoluene in 200 ml tetrahydrofuran is added dropwise to an ice-cold saturated solution of dimethylamine in 1 liter of tetrahydrofuran and the mixture stirred for 2 days at 25°. It is diluted with diethyl ether, washed with 2N aqueous sodium hydroxide, the organic layer dried, evaporated, the residue distilled and the fraction boiling at 106°/12 mm Hg collected, to yield the N,N-dimethyl-4-chlorobenzylamine.
Workup
- customThe starting material is prepared
- washwashed with 2N aqueous sodium hydroxide
- customthe organic layer dried
- customevaporated
- distillationthe residue distilled
- customthe fraction boiling at 106°/12 mm Hg collected
Sources & evidence
- ORD record
- ord-03212b35737c4e14a443ff8343bdb784
- Source dataset
- uspto-grants-1978_07
- Patent number
- US04099012
Reaction notes
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